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	<id>https://www.conservapedia.com/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Able806</id>
	<title>Conservapedia - User contributions [en]</title>
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	<updated>2026-10-01T03:44:30Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>https://www.conservapedia.com/index.php?title=User_talk:CPalmer&amp;diff=725950</id>
		<title>User talk:CPalmer</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=User_talk:CPalmer&amp;diff=725950"/>
		<updated>2009-12-02T13:32:31Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Longest basic rights */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;small&amp;gt;Archive: [[User talk:CPalmer/Archive2008|2008]] | [[User talk:CPalmer/Archive2009a|Jan-Apr 2009]]&amp;lt;/small&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==Bible quote text-popup==&lt;br /&gt;
{{QuoteBox|One of the best things about this site is that Bible references automatically show the text when you put the mouse over them. Example: Ezra 10:22.}}&lt;br /&gt;
That would be nice.  Unfortunately, it doesn't. :)&lt;br /&gt;
&lt;br /&gt;
(I don't know where to put this, so I'm putting it at the top)&lt;br /&gt;
- [[User:EvanW]] 31 Oct 09&lt;br /&gt;
&lt;br /&gt;
: Ah, yes. Well, it used to, and it may do again in the future. I assume it's a temporary bug.--[[User:CPalmer|CPalmer]] 11:27, 12 November 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
== &amp;quot;Decreasingly new&amp;quot; ==&lt;br /&gt;
&lt;br /&gt;
That made me laugh. I'm going to have to steal it now. [[User:Jinxmchue|Jinx McHue]] 11:51, 5 May 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:Thanks Jinx - steal away! It's funny, but I've been editing here for months and somehow I do still feel like the new guy.--[[User:CPalmer|CPalmer]] 11:59, 5 May 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
==Hahaha==&lt;br /&gt;
This wiki makes me laugh. Much like Fox News, it claims to be unbiased but instead portrays only one side of the situation. Can you possibly say the [[Barack Obama]] article is unbiased? Ahahahah. This wiki was supposedly created because Wikipedia was too biased in liberals' favor, but the funny thing is, this wiki is ten times more biased than Wikipedia could ever hope to be. [[User:Scarecrowk|Scarecrowk]]&lt;br /&gt;
:It's all very well to laugh, but perhaps you could work to improve what you think is lacking instead? New contributors are always welcome here.&lt;br /&gt;
:Also note that Conservapedia doesn't claim to be unbiased - it openly has a declared US conservative point of view. Otherwise it would have to be called Unbiasedopaedia!--[[User:CPalmer|CPalmer]] 07:49, 21 May 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::Right. Wikipedia says &amp;quot;we're neutral&amp;quot; and then they insert and defend bias. We basically say up front &amp;quot;we're biased!&amp;quot; which is not true bias, but declared POV. [[User:AddisonDM|AddisonDM]] 11:53, 21 May 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
==images==&lt;br /&gt;
File:NoSmoking.png, File:Ashtray.jpg. Here are the names of the images you requested about smoking. [[User:AddisonDM|AddisonDM]] 23:08, 29 May 2009 (EDT)&lt;br /&gt;
:Thanks Addison!--[[User:CPalmer|CPalmer]] 14:42, 3 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
== Thanks! ==&lt;br /&gt;
&lt;br /&gt;
Thanks for your edits this morning!--[[User:Aschlafly|Andy Schlafly]] 09:59, 11 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
: No problem - thanks for noticing!--[[User:CPalmer|CPalmer]] 10:21, 11 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
==Aditional Thanks==&lt;br /&gt;
&lt;br /&gt;
Thanks for helping clean my Metallicity article, I didn't realize I left that original extra paragraph in there, was using it to organize thoughts -- [[User:BMcP|BMcP]] 15:13, 18 June 2009 [EDT]&lt;br /&gt;
&lt;br /&gt;
==Ok Serious now==&lt;br /&gt;
If you agree to forget the past few minutes I will be constructive.  My interests include the Darwinian influence on morality and black holes.{{unsigned|Wheelchairman}}&lt;br /&gt;
:I'm not an administrator, so don't have authority to forget/not forget anything! If you'd like to improve pages on, say, [[sin]] or [[black hole]]s I'm sure that would be welcome.--[[User:CPalmer|CPalmer]] 10:06, 19 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
== The Vandal ==&lt;br /&gt;
&lt;br /&gt;
How can we get rid of the 'Wheelchairman' vandal? Could we email a sysop? [[User:JohnFraiser|JohnFraiser]] 10:01, 19 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
: You can try posting on sysops' talk pages or even emailing them, but to be honest if any were online they would probably notice the activity in &amp;quot;Recent changes&amp;quot; anyway. That leaves us with the standard tactics of reverting, ignoring or appealing to their better nature.--[[User:CPalmer|CPalmer]] 10:06, 19 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::Gosh, I thought I appeared to be &amp;quot;online&amp;quot;.  I'd better have Webmaster check it! Thank goodness Joaquin spotted it. --[[User:TK|'''ṬK''']]&amp;lt;sub&amp;gt;&amp;lt;small&amp;gt;&amp;lt;small&amp;gt;/Admin&amp;lt;/small&amp;gt;&amp;lt;/small&amp;gt;&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;[[User_Talk:TK|/Talk]]&amp;lt;/sup&amp;gt; 19:11, 19 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::I didn't see you in 'recent changes'. For future reference, do you get an alert automatically if someone posts on your page?--[[User:CPalmer|CPalmer]] 07:44, 20 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::::When your User talk page has a new edit, there should be a notice that appears in the upper right-hand corner of your screen view.  That's what I see.  Perhaps it is a profile setting.  Alternatively, you can always click on &amp;quot;Watch this page&amp;quot; for highlighting of an edit to any page.--[[User:Aschlafly|Andy Schlafly]] 08:02, 20 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::::I see a orange banner that says I have a &amp;quot;new&amp;quot; message, and links that either take me to the talk page, and another that takes me directly to the history &amp;quot;diff&amp;quot;. That is how I manage to watch CP and still reduce the backlog TiVo has on it! --[[User:TK|'''ṬK''']]&amp;lt;sub&amp;gt;&amp;lt;small&amp;gt;&amp;lt;small&amp;gt;/Admin&amp;lt;/small&amp;gt;&amp;lt;/small&amp;gt;&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;[[User_Talk:TK|/Talk]]&amp;lt;/sup&amp;gt; 08:10, 20 June 2009 (EDT)&lt;br /&gt;
::::::I get the 'new messages' banner as well - I was just wondering if the admins got alerted even if they weren't actually looking at Conservapedia at the time. We could have done with a 'bat signal' when that joker was about yesterday.--[[User:CPalmer|CPalmer]] 08:29, 20 June 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
== Vice President of the United States ==&lt;br /&gt;
&lt;br /&gt;
Thinking about this problematic title, shouldn't the link &amp;lt;noinclude&amp;gt;[[Vice President]]&amp;lt;/noinclude&amp;gt; go to an article and NOT a person, that changes or possibly does, every election cycle?  --[[User:TK|'''ṬK''']]&amp;lt;sub&amp;gt;&amp;lt;small&amp;gt;&amp;lt;small&amp;gt;/Admin&amp;lt;/small&amp;gt;&amp;lt;/small&amp;gt;&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;[[User_Talk:TK|/Talk]]&amp;lt;/sup&amp;gt; 15:47, 7 July 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:That would make sense, I think. Probably better for an American to write it though - we Brits don't have a vice-Queen!--[[User:CPalmer|CPalmer]] 07:59, 11 July 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Longest Running ==&lt;br /&gt;
User:FOIA has you beat by several months. You are the longest running Brit at CP. --[[User:Jpatt|Jpatt]] 12:10, 31 July 2009 (EDT)&lt;br /&gt;
:Ah, I suspected there would be somebody. Thanks for the heads-up, as I believe Americans often say.--[[User:CPalmer|CPalmer]] 08:42, 3 August 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
==Grammar==&lt;br /&gt;
&lt;br /&gt;
Thanks for [http://www.conservapedia.com/index.php?title=Conservative&amp;amp;curid=2849&amp;amp;diff=696646&amp;amp;oldid=696645&amp;amp;rcid=762970 this correction]. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:32, 28 August 2009 (EDT)&lt;br /&gt;
:You're welcome, although I did put the ungrammatical sentence in in the first place!--[[User:CPalmer|CPalmer]] 11:45, 28 August 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
== Thanks ==&lt;br /&gt;
&lt;br /&gt;
Thanks for your edit to [[conservative]]!  And thanks for your other superb work.  I've learned from your contributions.--[[User:Aschlafly|Andy Schlafly]] 11:10, 28 August 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:Quite welcome. As a Brit, I've been looking for a succinct definition to sum up US conservatism and that seemed to fit the bill.--[[User:CPalmer|CPalmer]] 11:37, 28 August 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::Britain seems to be swinging back to conservatism now.  I'm optimistic as entries like [[Essay:Best New Conservative Words]] indicate.  Regardless, thanks again for your insights.--[[User:Aschlafly|Andy Schlafly]] 12:28, 28 August 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::It's certainly likely that the Conservative Party will win the next election, though only some of their positions would be considered conservative by American standards. They do have some ideas on deregulating state education that you might find interesting.--[[User:CPalmer|CPalmer]] 12:39, 28 August 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
==Thanks again==&lt;br /&gt;
&lt;br /&gt;
I was editing [[dog meat]] at Wikipedia, and I absentmindedly inserted text for their article into our [[Windows bugs]] article. Thanks for that prompt correction; you saved me some embarassment; I looked like a graffiti artist for a moment there ;-) --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 11:31, 18 September 2009 (EDT)&lt;br /&gt;
:Don't mention it! It did look weird, but I knew there would be an explanation.--[[User:CPalmer|CPalmer]] 12:01, 18 September 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
== [[Conservative Bible Project]] ==&lt;br /&gt;
&lt;br /&gt;
Hi, there! In case you didn't know it, I've lately taken command of this Project, under the direct authority of Mr. [[User:Aschlafly|Schlafly]]. That generally means that if you're going to participate in it, I need to know your qualifications. Here are mine: I can read ancient Greek almost as fast as I can read modern English; the only limitation I have is in vocabulary, and I have a Strong's and a Newman's Concise Dictionary.&lt;br /&gt;
&lt;br /&gt;
If you would like to take on translating a whole book of the Bible, let me know. But all I ask is that people finish what they begin.--[[User:TerryH|TerryH]]&amp;lt;sup&amp;gt;[[User talk:TerryH|Talk]]&amp;lt;/sup&amp;gt; 14:59, 17 October 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:Hello Terry. I have just been looking to translate one verse each day, as much as an aid to my own understanding as a contribution to the project. Is this kind of low-key activity welcome, or should contributors make a more substantial commitment before getting involved at all?--[[User:CPalmer|CPalmer]] 09:40, 21 October 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
== Longest basic rights ==&lt;br /&gt;
&lt;br /&gt;
* 01:26, 24 March 2008 [[User:JLauttamus|JLauttamus]] (Talk | contribs) New user account ‎ &lt;br /&gt;
So hah!  -- [[User:JLauttamus|Jeff W. Lauttamus]][[User_talk:JLauttamus|&amp;lt;sub&amp;gt;Discussion&amp;lt;/sub&amp;gt;]] 13:58, 10 November 2009 (EST)&lt;br /&gt;
By the way, who's the first longest-running?  -- [[User:JLauttamus|Jeff W. Lauttamus]][[User_talk:JLauttamus|&amp;lt;sub&amp;gt;Discussion&amp;lt;/sub&amp;gt;]] 13:59, 10 November 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Congratulations! I'll amend the page accordingly. The other one is FOIA - I think it may be a close-run thing between the two of you.--[[User:CPalmer|CPalmer]] 11:05, 12 November 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Yeah, he's got me by about 15 days.  -- [[User:JLauttamus|Jeff W. Lauttamus]][[User_talk:JLauttamus|&amp;lt;sub&amp;gt;Discussion&amp;lt;/sub&amp;gt;]] 12:08, 12 November 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
:::I haven't been around quite that long, but I have been around since early May 2008.  --[[User:Benp|Benp]] 12:45, 27 November 2009 (EST)&lt;br /&gt;
::::Ah - thanks for letting me know. You've just got yourself a spot on the list.--[[User:CPalmer|CPalmer]] 07:28, 2 December 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:::::Just to add 15:19, 20 September 2007 Able806 (Talk | contribs) New user account ‎--[[User:Able806|Able806]] 08:32, 2 December 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=665394</id>
		<title>Nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=665394"/>
		<updated>2009-05-21T19:29:35Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Inosine */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose|2'-deoxyribose]], &lt;br /&gt;
and a  [[nitrogen]]ous base ([[pyrimidine]] or [[purine]]). The initial letters of the base names spell out the [[genetic code]]:&lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In [[DNA]] base pairing, adenine pairs with thymine, and guanine pairs with cytosine, while in [[RNA]] adenine pairs with uracil.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nitrogenous bases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidine monophosphate (TMP), Thymidine diphosphate (TDP) or Thymidine triphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine monophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nitrogenous bases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
===Inosine===&lt;br /&gt;
Inosine is derived from the two-ring parent molecule purine. Inosine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional carbonyl attached to the six-carbon ring. Inosine is found in tRNA and is essential for translation of the genetic code in wobble base pairs.&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=665393</id>
		<title>Nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=665393"/>
		<updated>2009-05-21T19:21:08Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Purine Nitrogenous bases */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose|2'-deoxyribose]], &lt;br /&gt;
and a  [[nitrogen]]ous base ([[pyrimidine]] or [[purine]]). The initial letters of the base names spell out the [[genetic code]]:&lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In [[DNA]] base pairing, adenine pairs with thymine, and guanine pairs with cytosine, while in [[RNA]] adenine pairs with uracil.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nitrogenous bases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidine monophosphate (TMP), Thymidine diphosphate (TDP) or Thymidine triphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine monophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nitrogenous bases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
===Inosine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=638266</id>
		<title>Talk:Significance of E. Coli Evolution Experiments</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=638266"/>
		<updated>2009-03-12T16:36:58Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;SJohnson, your assessment, while good in the utilization of the chi-squared test is unfortunately incorrect.  The Monte Carlo resampling gives a more accurate p-value than the chi-squared.  You may research the literature (i.e. publications in statistical mathematics, many pubs actualy compare Monte Carlo vs Chi Squared) to discover that this method is commonly used in advance statistical work and how it is more accurate than the chi-squared test.--[[User:Able806|Able806]] 17:00, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:It doesn’t make sense to compare the chi-square test, which is a specific statistical hypothesis test, to Monte Carlo methods, which can be used for anything from fluid motion modeling to p-value computations. You can use Monte Carlo methods to compute the p-values of the chi-square test!&lt;br /&gt;
&lt;br /&gt;
:Monte Carlo methods involve the generation of random realizations. Your broad claim the Monte Carlo methods are “more accurate” than the chi-square test is obviously incorrect because the accuracy of Monte Carlo methods always depends on the number of random realizations generated. When p-values are small, Monte Carlo methods are notoriously inaccurate unless the number of realizations generated is enormous.&lt;br /&gt;
&lt;br /&gt;
:Which publications compare Monte Carlo to chi-square and show that the former is more accurate? Could you provide specific examples? Thanks.  [[User:SJohnson|SJohnson]] 18:50, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:In furtherance of SJohnson's remarks with respect to rarely occurring events, the use of the basic Monte Carlo method is plainly incorrect for modeling a rarely occurring event, as the Lenski paper did.  This has long been pointed out in [[Flaws in Richard Lenski Study]].  I know [[evolutionists]] will never admit a flaw in anything promoting their pet theory, but this (and other) flaws in that paper is undeniable.&lt;br /&gt;
&lt;br /&gt;
:Watch how evolutionists defended obvious errors in the Lenski paper, and then realize why the [[Piltdown Man]] fraud was taught for 40 years without evolutionists admitting it was a hoax.--[[User:Aschlafly|Andy Schlafly]] 09:55, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Andy, how exactly is the Monte Carlo method incorrect to use in this case?  I have seen it used in publications with much smaller datasets.--[[User:Able806|Able806]] 10:29, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:::Able806, I'm interested in looking at the publications you mentioned that use Monte Carlo methods to analyze small data sets. Could you provide some examples? Thanks. [[User:SJohnson|SJohnson]] 16:41, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::SJohnson, here are two papers, [http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6WH8-45RFJ1J-19&amp;amp;_user=10&amp;amp;_rdoc=1&amp;amp;_fmt=&amp;amp;_orig=search&amp;amp;_sort=d&amp;amp;view=c&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=1ad95954654bb97b17e474ce6b469f6e 1] and [http://cat.inist.fr/?aModele=afficheN&amp;amp;cpsidt=787963 2].  Most are in chemistry and genetics where you find the observed to be much smaller and have to use the MCM.  You can search on the subject as well and find that how Lenski performed the test is the standard for microbiological genetic analysis.--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::::Those papers have nothing to do with hypothesis testing. One is an archeology paper. To be blunt, it seems like you’re just doing internet searches on “Monte Carlo” to find these links. [[User:SJohnson|SJohnson]] 10:10, 12 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::::::SJohnson, actually they do, did you read the papers?  If so you would see how they used the MCM for their data analysis of small data sets, which indeed was hypothesis testing and answers you inquiry about publications that use MCM for small data set analysis.  If you wish I can try to track down some actual mathematical publications, however, I am not as familiar with mathematical journals as I am with science/medical journals (not knowing which mathematical journals are acceptable).  I am assuming that you have a background in math and possibly access to mathematical journals, therefore if you know the reputable ones I can do the leg work. &lt;br /&gt;
::::::I believe the thing that needs to be looked at is there truly a problem with the choice of test and if so what is an alternative.  Bayesian might be an option but seems to be difficult to employ for this situation.--[[User:Able806|Able806]] 12:36, 12 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::Able806, you still seem to miss the point about how inappropriate the Monte Carlo method (as used in the Lenski paper) is for evaluating rarely occurring events.  You need to open your mind to be productive.  If you simply cling to a view that Lenski (who I don't think has any meaningful education in statistics) must somehow be right, then you're not going to make any progress in understanding the flaws.--[[User:Aschlafly|Andy Schlafly]] 17:07, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::Andy, you still have not answered what you find inappropriate about his use of the Monte Carlo method?  I am a reasonable person and with evidence I do have an open mind.  I provided examples last week, with a working model, showing that Monte Carlo is better than the chi-square in this case.  I have also shown where the Chi-Square was inappropriate due to the occurrence size as well. So if you have any evidence that Monte Carlo should not be used in the way that Lenski used please let it be shown.--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)  &lt;br /&gt;
&lt;br /&gt;
Sjohnson, I believe you just proved my point.  In the literature of mean and covariance structure analysis, non-central chi-square distribution is commonly used to describe the behavior of the likelihood ratio statistic under alternative hypothesis; it is widely believed that the non-central chi-square distribution is justified by statistical theory. Actually, when the null hypothesis is not trivially violated, the non-central chi-square distribution cannot describe the LR statistic well even when data are normally distributed and the sample size is large. Monte Carlo results compare the strength of the normal distribution against that of the non-central chi-square distribution.  In an association analysis comparing cases and controls with respect to allele frequencies at a highly polymorphic locus, a potential problem is that the conventional chi-squared test may not be valid for a large, sparse contingency table. Reliance on statistics with known asymptotic distribution is unnecessary, as Monte Carlo simulations can be performed to estimate the significance level of the test statistic.&lt;br /&gt;
&lt;br /&gt;
Here is a [http://faculty.vassar.edu/lowry/chi_beta.html  link] to a great page the provides an interactive example as to why the Chi Squared test would provide poor results compared to the Monte Carlo in relation to the Lenski data workup.  &lt;br /&gt;
&lt;br /&gt;
Something you may have overlooked was that the data set is actually too small to use the chi square method correctly.  It is often accepted that is any of the analyzed data falls under 10 for a particular cell of the data set then the Yates correction needs to be applied; unfortunately the Yates correction can over correct thus skewing the p-value.  Lenksi seemed to understand this by supporting his Monte Carlo p-value results with the Fisher z-transformation p-value.&lt;br /&gt;
&lt;br /&gt;
I hope this helps.--[[User:Able806|Able806]] 10:27, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:I’m still waiting to hear which literature says that “Monte Carlo resampling” is “more accurate than the chi-squared test”. The page mentioned above [http://faculty.vassar.edu/lowry/chi_beta.html] is a discussion of why statisticians “fail to reject the null” rather than “accepting the null” when the p-value is above 0.05 or so. The page says nothing about superiority of Monte Carlo methods. Why were alternate hypothesis distributions mentioned? Only the null hypothesis distribution is used to calculate a p-value. Yates’s correction is for 2x2 contingency tables [http://en.wikipedia.org/wiki/Yates%27_correction_for_continuity]. It doesn’t apply in this case. Finally, what the heck do “covariance structure analysis” and “allele frequencies at a highly polymorphic locus” have to do with this problem? [[User:SJohnson|SJohnson]] 16:38, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::SJohnson, I am looking for this paper for you, I cited it for one of my past publications dealing with allele frequencies (I believe it came from the Duke Biostatistics group).  To answer your question about allele frequencies, that is the issue at hand, more about the genetics than the math, but it is the item being studied.  So you stated that Yates can not be used and statistics says the number of occurrences is too small to evaluate using the Chi-Squared test so what would you recommend instead of the Monte-Carlo Method?&lt;br /&gt;
&lt;br /&gt;
:Regarding the &amp;quot;Fisher z-transformation p-value&amp;quot; from the paper, garbage in garbage out. If the p-values were bad to begin with, then why would a combination of them be meaningful? [[User:SJohnson|SJohnson]] 10:49, 9 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::You are assuming that p-values are wrong based on a test that is inappropriate in this case due to data limitations.  Did you perform a z-transformation on the chi-squared for the three data groups?--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::You asked about the “Fisher z-transformation p-value”. The z-transformation test and Fisher’s method are actually two different things (see Whitlock's 2005 paper - Ref. 49 in Blount et al.). But no, I haven’t tried either. [[User:SJohnson|SJohnson]] 10:10, 12 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::There's a large literature on various kinds of Monte Carlo test, a very short summary of which is that they're inevitably more accurate than parametric tests (e.g. F, t, chi-squared, etc) because they don't make assumptions about the distribution of the data under the null hypothesis. See for example ''Introduction to the Bootstrap'' by B. Efron and R. Tibshirani and ''The Jack-knife, the Bootstrap and Other Resampling Plans'', also by Efron. They're certainly applicable to small datasets and their accuracy is really only limited by the number of samples you care to take. E.g. 1000 M-C samples would give you a pretty accurate idea about significance at the alpha&amp;lt;1% level (That book should answer SJohnson's questions of 18:50 on 4/3/09 and 16:38 on 5/3/09 about accuracy and Aschalfly's comment of 17:07 on 5/3/09 about appropriateness of Monte Carlo tests.) [[User:FredFerguson|FredFerguson]] 16:53, 11 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::::Your claim that Monte Carlo methods are “inevitably more accurate” than other tests is obviously wrong because the accuracy of MC methods always depends on the number of realizations used. You should have written &amp;lt;math&amp;gt;\alpha=1\%&amp;lt;/math&amp;gt;, not &amp;lt;math&amp;gt;\alpha&amp;lt;1\%&amp;lt;/math&amp;gt;. If 1,000 random realizations are generated, the number of realizations above the true &amp;lt;math&amp;gt;\alpha=1\%&amp;lt;/math&amp;gt; level is binomial with mean 10 and variance about 10. Thus, the standard deviation of the MC estimate is &amp;gt;0.003. In this example, a Monte Carlo p-value could be off by 30% and still be within a standard deviation. Is that really “pretty accurate”?&lt;br /&gt;
&lt;br /&gt;
::::Using one million MC realizations (as done in the paper) at the &amp;lt;math&amp;gt;\alpha=0.001&amp;lt;/math&amp;gt; level means the standard deviation is about 10%. The paper reported a p-value of less than 0.001 (experiment two). It wouldn’t surprise me to find out that the experiment two p-value for the flawed test is off because only one million realizations were used. My original statement, “When p-values are small, Monte Carlo methods are notoriously inaccurate unless the number of realizations generated is enormous” is correct. [[User:SJohnson|SJohnson]] 10:10, 12 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::::You're talking about miniscule differences in the accuracy of a test. 0.013 isn't very different from 0.007. In either case, it's very unlikely the experimenter would have obtained that result if the null hypothesis were true. If you're bothered about differences in P-values to the third decimals (which would make you unusual!), just run more MC realisations, that's all. Not really a problem. [[User:FredFerguson|FredFerguson]] 11:53, 12 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
There’s still confusion about the difference between test statistics and Monte Carlo methods. Before you find a Monte Carlo estimate of a p-value, you need to select a test statistic to reduce the data set to a scalar. I am interested in hearing which test statistic you believe should be used in place of the chi-square test and why. [[User:SJohnson|SJohnson]] 10:10, 12 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
Quick question for SJohnson: How many degrees of freedom did you choose when calculating the p-value? I'd like to know upon what condition you base that number. Thanks.--[[User:Argon|Argon]] 11:05, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:The degree of freedom for a contingency table is rows minus one times columns minus one. That is, &amp;lt;math&amp;gt; (r-1)(c-1) &amp;lt;/math&amp;gt;. Here’s a pretty good tutorial I came across: [http://faculty.uncfsu.edu/dwallace/lesson%2020.pdf]. For the experiments from [http://www.pnas.org/content/105/23/7899.full.pdf], the DOFs are 11, 11, and 13. For experiment one, the chi-square test statistic is&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
X^2&lt;br /&gt;
=\sum\limits_i\sum\limits_j&lt;br /&gt;
\frac{\left(n_{i,j}-E\left[n_{i,j}\right]\right)^2}&lt;br /&gt;
{E\left[n_{i,j}\right]}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
=\frac{\left(0-1/3\right)^2}{1/3}&lt;br /&gt;
+\frac{\left(6-17/3\right)^2}{17/3}&lt;br /&gt;
+\frac{\left(0-1/3\right)^2}{1/3}&lt;br /&gt;
+\ldots+&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
+\frac{\left(2-1/3\right)^2}{1/3}&lt;br /&gt;
+\frac{\left(4-17/3\right)^2}{17/3}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
\approx&lt;br /&gt;
14.82&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
:where &amp;lt;math&amp;gt;n_{i,j}&amp;lt;/math&amp;gt; is the observed value and &amp;lt;math&amp;gt;E\left[n_{i,j}\right]&amp;lt;/math&amp;gt; is the expected null hypothesis value. So if you have MS Excel, another way to arrive at the p-value of 0.19 is to type “=CHIDIST(14.82,11)” into a cell. Cheers! [[User:SJohnson|SJohnson]] 16:38, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::OK, thanks for the info. From what I'd calculated and looked up in tables, the numbers seemed close to a df=11 for a chi-square of ~14. (Aside: With terms having 17/3 in the denominator in the figures above, were you using the test of independence? I was using Pearson's test for [http://en.wikipedia.org/wiki/Pearson%27s_chi-square_test#Test_for_fit_of_a_distribution fit of a distribution] which returns a chi-squared value of 14 and roughly matched the p-values you reported, assuming the df was 11).&lt;br /&gt;
&lt;br /&gt;
::Also, the first sentence of the article reads: &amp;quot;Blount, Borland, and Lenski[1] claimed that a key evolutionary innovation was observed during a laboratory experiment. That claim is false.&amp;quot; A small correction: There were several claims in the paper. The 'key evolutionary innovation' was acquiring the ability to utilize citrate as a food source. That claim was demonstrated multiple times. The claim, which pertains to this statistics discussion was that the Cit+ phenotype arose in a multi-step process, first requiring a rare, pre-adaptive mutation before additional mutation(s) lead to the subsequent development of citrate utilization.--[[User:Argon|Argon]] 20:46, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:::My biology-degreed wife assures me that mutation does not necessarily mean that evolution occurred. What the paper claimed is that evolution (a “key innovation”) occurred in the lab. The key innovation supposedly increased the mutation rate. In the experiments, the observed mutation rate increased after generation 31,000, but not enough to make a statistically significant claim that the rate is not constant. The analysis in the paper was similar to flipping a coin ten times, counting six heads and claiming that the coin must be biased against tails. In reality, there’s nothing surprising about a fair coin producing slightly more of one outcome than the other. Just like there's nothing surprising about there being slightly more mutations in later generations than early generations given the null hypothesis (constant mutation rate). [[User:SJohnson|SJohnson]] 10:46, 9 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::::SJohnson, not to say anything about your wife, but has she had a 400 level molecular genetics course (most general biology degrees do not cover the detail unless they are specialized)?  If so, she would have mentioned that if the mutation passes to the offspring and is selectively beneficial to the population then it is a step of evolution as along as the conditions continue through the sharing of the mutation with the population and the environment is such that reduces the growth rate of the non-transformed population.  While not all mutations are signs that evolution occurred the mutations that pass to offspring and provide a benefit compared to other offspring are very strong indicators.  In the case of this paper the population that evolved the cit+ was able to metabolize a chemical in their environment which allowed for an adaptation advantage compared to the non-transformed colonies.--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
Let’s go back to the beginning. There appears to be confusion about the difference between test statistics and methods for computing p-values. As is noted at the beginning of the page [http://www.conservapedia.com/Significance_of_E._Coli_Evolution_Experiments], the fundamental problem with the paper is that it used a flawed test statistic, not that it used Monte Carlo methods to find the p-value for that flawed statistic.&lt;br /&gt;
&lt;br /&gt;
Every hypothesis test uses a test statistic to reduce the data to a single number. The p-value for the test statistic can be calculated analytically (as I’ve done for the chi-square test statistic) or by Monte Carlo methods. In the paper, Monte Carlo methods were used to compute the p-value of the “mutation generation” test statistic. The key problem with the analysis from the paper is that it doesn’t work to use a weighted average to test for variations in mutation rate. This is like trying to use the sample variance to test for an increase in the mean in Gaussian-distributed data. A statistic should be selected based on the null and alternate hypothesis distributions of the data. The chi-square test (unlike the weighted average from the paper) is a reasonable choice for data that mutates at a constant rate under the null hypothesis, but mutates at varying rates under the alternate hypothesis.&lt;br /&gt;
&lt;br /&gt;
Able806, you made a good point about the contingency table cell frequencies being relatively low, but were wrong when you said ”the data set is actually too small to use the chi square method correctly”. In the low cell frequency case the chi-square test is still effective, but the null hypothesis distribution of the chi-square statistic starts to look less like the chi-square distribution. Thus, p-values calculated using the chi-square distribution may be a bit off. However, Monte Carlo p-values are always imperfect as well because it's impossible to generate an infinite number of random realizations. There are imperfections in p-values generated by analytic and Monte Carlo methods. However, low cell frequencies does not explain the &amp;gt;20x and &amp;gt;2.5x differences between chi-square p-values and p-values from the paper for experiments one and three. The reason for those huge differences was the use of the flawed test statistic (“mutation generation”) in the paper. [[User:SJohnson|SJohnson]] 16:38, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:SJohnson, the chi-squared test is a valuable statistical tool, but the limitations of the test must be acknowledged. The chi-squared test can only produce valid results if the assumptions that underly the test are not violated. As an analogy, Newtonian models of motion fail to produce accurate results as velocities approach the speed of light; under those circumstances one must switch to a theory that accounts for relativistic effects.&lt;br /&gt;
&lt;br /&gt;
:It seems that you have simply dismissed the [http://www.okstate.edu/ag/agedcm4h/academic/aged5980a/5980/newpage28.htm widely-acknowledged] [http://faculty.chass.ncsu.edu/garson/PA765/chisq.htm fact] that the [http://www.wellesley.edu/Psychology/Psych205/chisquareindep.html chi-squared test] is [http://www.minitab.com/support/answers/answer.aspx?log=0&amp;amp;id=2236 inappropriate] for use in [http://www.graphpad.com/www/Book/Choose.htm situations] where n in any cell is [http://mysite.du.edu/~jcalvert/econ/chisquar.htm less] less than a [http://books.google.com/books?id=yU15rUiLRI8C&amp;amp;pg=PA201&amp;amp;lpg=PA201&amp;amp;dq=chi-square+test+assumptions&amp;amp;source=bl&amp;amp;ots=FRY0LwQ3z_&amp;amp;sig=FyIvzJx3hjQ8nWlu2cpmZj3pwXY&amp;amp;hl=en&amp;amp;ei=fm-1SayaNI_MMKX5tO4E&amp;amp;sa=X&amp;amp;oi=book_result&amp;amp;ct=result#PPA185,M1 threshold] [http://www.basic.northwestern.edu/statguidefiles/gf-dist_ass_viol.html number]. Different authors set different thresholds, but all are well above the numbers seen in your chi-squared analysis - even the most liberal guidelines advise against the chi-squared test when any expected cell frequency is less than one or more than 20% of the table cells are less than 5; others require that expected values in all cells must be more than 5. With smaller amounts of data, the test is insensitive and errs on the side of rejecting the hypothesis. If you attempt your chi-squared statistical analysis with a program that is more sophisticated than MS Excel (as I did), you get an error message indicating that the results are invalid due to low expected cell counts.&lt;br /&gt;
&lt;br /&gt;
:That issue aside, there are other reasons that the chi-squared test is inappropriate here. As the links above point out, the categories tested must be truly independent; one example is that you can't use the chi-squared test to compare age and ability to kick a field goal by testing the same experimental group twice, one year apart; you have to test one group of age A and a different group of age B. In the case of the Blount paper, the categories are not independent. Even if there were adequate numbers to address the low-expected-frequency problem, this would make the chi-squared an invalid test in this case.&lt;br /&gt;
&lt;br /&gt;
:There are other significant problems with the use of the chi-squared test in this circumstance, but they can wait until you address these first major problems.--[[User:ElyM|ElyM]] 12:18, 11 March 2009 (EDT)  &lt;br /&gt;
&lt;br /&gt;
::Wackerly et al. says in general it’s assumed that the cell frequencies are above five so that the chi-square statistic (under the null) is approximately chi-square distributed (see p. 703). That book does not say chi-square test results are invalid if frequencies are five or less. Your example of a chi-square test warning message (it said &amp;quot;warning&amp;quot; not &amp;quot;error&amp;quot; as you stated) in Minitab [http://www.minitab.com/support/answers/answer.aspx?log=0&amp;amp;id=2236] said “approximation probably invalid” referring to the chi-square distribution approximation to the chi-square test statistic’s distribution. Your example did not say “chi-square test invalid”. I agree that when cell frequencies are low, the chi-square test statistic’s distribution starts to deviate from the chi-square distribution. I maintain that this deviation is not enough to explain the &amp;gt;2.5x and &amp;gt;20x differences in the chi-square test p-values and the p-values from the paper.&lt;br /&gt;
&lt;br /&gt;
::As the numerous links in your post proved, the chi-square test is widely-used by statisticians. Can you give examples of statisticians using mean mutation generation as a test statistic? Also, did your software agree with the chi-square test p-values I presented? Thanks. [[User:SJohnson|SJohnson]] 10:10, 12 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
== Misinterpretation of test ==&lt;br /&gt;
&lt;br /&gt;
SJohnson, Your analysis misinterprets the test. You say the null hypothesis is that this mutation cannot happen. They saw a mutation (4 mutations, in fact, in the data set you show) so the null hypothesis (as you state is) is disproved. That's perfectly straightforward.&lt;br /&gt;
&lt;br /&gt;
I don't know what the &amp;quot;mean mutation generation&amp;quot; test is but you're doing when you apply a chi-squared test to this dataset is to test if the mutations are evenly distributed throughout the generations. Your test says they are, so there's no strong evidence to suppose that mutations are likely to occur in one generation rather than another in the series of tests. Blount's test says thay aren't, so it's more likely that the mutation will occur later in the series of tests. I can't tell which test is right without knowing more about the test that Blount used.&lt;br /&gt;
&lt;br /&gt;
But that point (the foregoing paragraph) has no bearing at all on the null hypothesis, as you describe it. The mutation appeared, so that means the hypothesis that the mutation can't happen is disproved. Very simple. [[User:FredFerguson|FredFerguson]] 21:10, 8 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:I never said that “the null hypothesis is that this mutation cannot happen”. The chi-square test statistic I'm using wouldn’t be defined if the null hypothesis mutation rate was zero because the &amp;lt;math&amp;gt;E\left[n_{i,j}\right]&amp;lt;/math&amp;gt; term in the denominator of the statistic (see above equation) would be zero.&lt;br /&gt;
&lt;br /&gt;
:The test statistic from the paper is the average of the generation numbers of observed mutations. For experiment one this number is&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
\frac{1}{4}\left(30500+31500+2\times32500\right)= 31750.&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
:The same number is shown in Table 2 of the paper. [[User:SJohnson|SJohnson]] 10:46, 9 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:: SJohnson, the way you're calculating the chi-squared statistic implies that you're testing the null hypothesis of a constant mutation rate over time against an alternative hypothesis of a mutation rate which varies over time. [[User:FredFerguson|FredFerguson]] 11:02, 9 March 2009 (EDT)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Blood&amp;diff=637730</id>
		<title>Blood</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Blood&amp;diff=637730"/>
		<updated>2009-03-11T14:35:40Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;'''Blood''' is a fluid that transports [[oxygen]] from the [[lungs]] to body tissue and [[carbon dioxide]] from body tissue to the lungs. Blood also transports nourishment from digestion and hormones from glands to all areas of the body. Blood also conveys disease fighting subtances to the tissues and waste to the kidneys. Blood is thicker than water and has a slightly salty taste. An adults body usually has 10 pints of blood circulating around. Blood is composed of billions of living blood cells floating in a liquid called plasma. If you took a small sample of this blood and poured it into a test tube and then put it in a machine called a centrifuge, you would be able to see the layers of this blood. This machine spins the blood around so fast that it separates the [[red blood cells]], from the [[white blood cells]], from the [[platelets]]. The red blood cells sink to the bottom because they are the heavier, more solid parts, but the plasma remains at the top because it is lighter. Plasma is 95% water and the other 5% is made up of dissolved substances including salts.&lt;br /&gt;
&lt;br /&gt;
==Origins of blood in the body==&lt;br /&gt;
All of the cellular elements of blood, including the red blood cells that transport oxygen, the platelets that trigger blood clotting in damaged tissues, and white blood cells of the immune system, derive ultimately from the same progenitor or precursor cells, the hematopoietic stem cells in the bone marrow.  As these stem cells can give rise to all of the different types of blood cells they are often known as pluripotent hematopoirtic stem cells.  Initially they give rise to stem cells of more limited potential, which are the immediate progenitors of red blood cells, platelets, and the two main categories of white blood cells.&lt;br /&gt;
&lt;br /&gt;
==Blood in the Bible==&lt;br /&gt;
After the [[Great Flood]], [[God]] commanded [[Noah]] as follows:&lt;br /&gt;
&lt;br /&gt;
{{Bible quote|But flesh with the life thereof, [which is] the blood thereof, shall ye not eat. And surely your blood of your lives will I require; at the hand of every beast will I require it, and at the hand of man; at the hand of every man's brother will I require the life of man. Whoso sheddeth man's blood, by man shall his blood be shed: for in the image of God made he man.|book=Genesis|chap=9|verses=4-6|version=KJV}}&lt;br /&gt;
&lt;br /&gt;
This commandment was part of the [[Noahide laws]] rather than the [[Mosaic law]] and was thus binding on all people.&lt;br /&gt;
&lt;br /&gt;
The Book of [[Acts]] in the [[New Testament]] reaffirmed the prohibition on eating blood:&lt;br /&gt;
&lt;br /&gt;
{{Bible quote|But that we write unto them, that they abstain from pollutions of idols, and [from] fornication, and [from] things strangled, and [from] blood.|book=Acts|chap=15|verses=20|version=KJV}}&lt;br /&gt;
&lt;br /&gt;
{{Bible quote|For it seemed good to the Holy Ghost, and to us, to lay upon you no greater burden than these necessary things; That ye abstain from meats offered to idols, and from blood, and from things strangled, and from fornication: from which if ye keep yourselves, ye shall do well. Fare ye well.|book=Acts|chap=15|verses=28-29|version=KJV}}&lt;br /&gt;
&lt;br /&gt;
[[Jehovah's Witnesses]] believe that [[blood transfusions]] are forbidden by God in the above passages from Acts.&lt;br /&gt;
&lt;br /&gt;
The shedding of blood is also necessary for the remission of [[sin]]:&lt;br /&gt;
&lt;br /&gt;
{{Bible quote|And almost all things are by the law purged with blood; and without shedding of blood is no remission.|book=Hebrews|chap=9|verses=22|version=KJV}}&lt;br /&gt;
&lt;br /&gt;
In the [[Old Testament]], this meant [[animal]] [[sacrifice]]s.  In the New Testament, it means the Blood of [[Christ]].&lt;br /&gt;
[[Category:biology]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637725</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637725"/>
		<updated>2009-03-11T14:28:05Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* History */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
When Jenner introduced vaccination he knew nothing of the infectious agents that cause disease: it was not until late in the 19th century that Robert Kock proved that infectious diseases are caused by microorganisms, each one responsible for a particular disease, or pathology.  We now recognize four broad categories of disease-causing [[microorganism]]s, or [[pathogen]]s: these are [[virus]]es; [[bacteria]]; pathogenic [[fungi]]; and other relatively large and complex eukaryotic organisms collectively termed [[parasite]]s.&lt;br /&gt;
&lt;br /&gt;
The discoveries of Koch and other great 19th century microbiologists stimulated the extension of Jenner's strategy of vaccination to other diseases.  In the 1880's, [[Louis Pasteur]] devised a vaccine against cholera in chickens, and developed a rabies vaccine that proved a success upon its first trial use in a boy bitten by a rabid dog.  These practical triumphs led to a search for the mechanism of protection and to the development of the science of immunology.  In 1890, Emil von Behring and Shibasaburo Kitasato discovered that the serum of vaccinated individuals contained substances, which they called [[antibodies]], that specifically bound to the relevant pathogen.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
[[Koch's postulates]]&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637724</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637724"/>
		<updated>2009-03-11T14:27:11Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* History */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
When Jenner introduced vaccination he knew nothing of the infectious agents that cause disease: it was not until late in the 19th century that Robert Kock proved that infectious diseases are caused by microorganisms, each one responsible for a particular disease, or pathology.  We now recognize four broad categories of disease-causing [[microorganism]]s, or [[pathogen]]s: these are [[virus]]es; [[bacteria]]; pathogenic [[fungi]]; and other relatively large and complex eukaryotic organisms collectively termed [[parasite]]s.&lt;br /&gt;
&lt;br /&gt;
The discoveries of Koch and other great 19th century microbiologists stimulated the extension of Jenner's strategy of vaccination to other diseases.  In the 1880's, [[Louis Pasteur]] devised a vaccine against cholera in chickens, and developed a rabies vaccine that proved a success upon its first trial use in a boy bitten by a rabid dog.  These practical triumphs led to a search for the mechanism of protection and to the development of the science of immunology.  In 1890, Emil von Behring and Shibasaburo Kitasato discovered that the serum of vaccinated individuals contained substances, which they called antibodies, that specifically bound to the relevant pathogen.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
[[Koch's postulates]]&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637723</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637723"/>
		<updated>2009-03-11T14:24:25Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
When Jenner introduced vaccination he knew nothing of the infectious agents that cause disease: it was not until late in the 19th century that Robert Kock proved that infectious diseases are caused by microorganisms, each one responsible for a particular disease, or pathology.  We now recognize four broad categories of disease-causing [[microorganism]]s, or [[pathogen]]s: these are [[virus]]es; [[bacteria]]; pathogenic [[fungi]]; and other relatively large and complex eukaryotic organisms collectively termed [[parasite]]s.&lt;br /&gt;
&lt;br /&gt;
The discoveries of Koch and other great 19th century microbiologists stimulated the extension of Jenner's strategy of vaccination to other diseases.  In the 1880's, [[Louis Pasteur]] devised a vaccine against cholera in chickens, and developed a rabies vaccine that proved a success upon its first trial use in a boy bitten by a rabid dog.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
[[Koch's postulates]]&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637722</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=637722"/>
		<updated>2009-03-11T14:22:01Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* History */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
When Jenner introduced vaccination he knew nothing of the infectious agents that cause disease: it was not until late in the 19th century that Robert Kock proved that infectious diseases are caused by microorganisms, each one responsible for a particular disease, or pathology.  We now recognize four broad categories of disease-causing [[microorganism]]s, or [[pathogen]]s: these are [[virus]]es; [[bacteria]]; pathogenic [[fungi]]; and other relatively large and complex eukaryotic organisms collectively termed [[parasite]]s.&lt;br /&gt;
&lt;br /&gt;
The discoveries of Koch and other great 19th century microbiologists stimulated the extension of Jenner's strategy of vaccination to other diseases.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
[[Koch's postulates]]&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=637721</id>
		<title>Talk:Significance of E. Coli Evolution Experiments</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=637721"/>
		<updated>2009-03-11T14:19:47Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;SJohnson, your assessment, while good in the utilization of the chi-squared test is unfortunately incorrect.  The Monte Carlo resampling gives a more accurate p-value than the chi-squared.  You may research the literature (i.e. publications in statistical mathematics, many pubs actualy compare Monte Carlo vs Chi Squared) to discover that this method is commonly used in advance statistical work and how it is more accurate than the chi-squared test.--[[User:Able806|Able806]] 17:00, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:It doesn’t make sense to compare the chi-square test, which is a specific statistical hypothesis test, to Monte Carlo methods, which can be used for anything from fluid motion modeling to p-value computations. You can use Monte Carlo methods to compute the p-values of the chi-square test!&lt;br /&gt;
&lt;br /&gt;
:Monte Carlo methods involve the generation of random realizations. Your broad claim the Monte Carlo methods are “more accurate” than the chi-square test is obviously incorrect because the accuracy of Monte Carlo methods always depends on the number of random realizations generated. When p-values are small, Monte Carlo methods are notoriously inaccurate unless the number of realizations generated is enormous.&lt;br /&gt;
&lt;br /&gt;
:Which publications compare Monte Carlo to chi-square and show that the former is more accurate? Could you provide specific examples? Thanks.  [[User:SJohnson|SJohnson]] 18:50, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:In furtherance of SJohnson's remarks with respect to rarely occurring events, the use of the basic Monte Carlo method is plainly incorrect for modeling a rarely occurring event, as the Lenski paper did.  This has long been pointed out in [[Flaws in Richard Lenski Study]].  I know [[evolutionists]] will never admit a flaw in anything promoting their pet theory, but this (and other) flaws in that paper is undeniable.&lt;br /&gt;
&lt;br /&gt;
:Watch how evolutionists defended obvious errors in the Lenski paper, and then realize why the [[Piltdown Man]] fraud was taught for 40 years without evolutionists admitting it was a hoax.--[[User:Aschlafly|Andy Schlafly]] 09:55, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Andy, how exactly is the Monte Carlo method incorrect to use in this case?  I have seen it used in publications with much smaller datasets.--[[User:Able806|Able806]] 10:29, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:::Able806, I'm interested in looking at the publications you mentioned that use Monte Carlo methods to analyze small data sets. Could you provide some examples? Thanks. [[User:SJohnson|SJohnson]] 16:41, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::SJohnson, here are two papers, [http://www.sciencedirect.com/science?_ob=ArticleURL&amp;amp;_udi=B6WH8-45RFJ1J-19&amp;amp;_user=10&amp;amp;_rdoc=1&amp;amp;_fmt=&amp;amp;_orig=search&amp;amp;_sort=d&amp;amp;view=c&amp;amp;_acct=C000050221&amp;amp;_version=1&amp;amp;_urlVersion=0&amp;amp;_userid=10&amp;amp;md5=1ad95954654bb97b17e474ce6b469f6e 1] and [http://cat.inist.fr/?aModele=afficheN&amp;amp;cpsidt=787963 2].  Most are in chemistry and genetics where you find the observed to be much smaller and have to use the MCM.  You can search on the subject as well and find that how Lenski performed the test is the standard for microbiological genetic analysis.--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:::Able806, you still seem to miss the point about how inappropriate the Monte Carlo method (as used in the Lenski paper) is for evaluating rarely occurring events.  You need to open your mind to be productive.  If you simply cling to a view that Lenski (who I don't think has any meaningful education in statistics) must somehow be right, then you're not going to make any progress in understanding the flaws.--[[User:Aschlafly|Andy Schlafly]] 17:07, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::Andy, you still have not answered what you find inappropriate about his use of the Monte Carlo method?  I am a reasonable person and with evidence I do have an open mind.  I provided examples last week, with a working model, showing that Monte Carlo is better than the chi-square in this case.  I have also shown where the Chi-Square was inappropriate due to the occurrence size as well. So if you have any evidence that Monte Carlo should not be used in the way that Lenski used please let it be shown.--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)  &lt;br /&gt;
&lt;br /&gt;
Sjohnson, I believe you just proved my point.  In the literature of mean and covariance structure analysis, non-central chi-square distribution is commonly used to describe the behavior of the likelihood ratio statistic under alternative hypothesis; it is widely believed that the non-central chi-square distribution is justified by statistical theory. Actually, when the null hypothesis is not trivially violated, the non-central chi-square distribution cannot describe the LR statistic well even when data are normally distributed and the sample size is large. Monte Carlo results compare the strength of the normal distribution against that of the non-central chi-square distribution.  In an association analysis comparing cases and controls with respect to allele frequencies at a highly polymorphic locus, a potential problem is that the conventional chi-squared test may not be valid for a large, sparse contingency table. Reliance on statistics with known asymptotic distribution is unnecessary, as Monte Carlo simulations can be performed to estimate the significance level of the test statistic.&lt;br /&gt;
&lt;br /&gt;
Here is a [http://faculty.vassar.edu/lowry/chi_beta.html  link] to a great page the provides an interactive example as to why the Chi Squared test would provide poor results compared to the Monte Carlo in relation to the Lenski data workup.  &lt;br /&gt;
&lt;br /&gt;
Something you may have overlooked was that the data set is actually too small to use the chi square method correctly.  It is often accepted that is any of the analyzed data falls under 10 for a particular cell of the data set then the Yates correction needs to be applied; unfortunately the Yates correction can over correct thus skewing the p-value.  Lenksi seemed to understand this by supporting his Monte Carlo p-value results with the Fisher z-transformation p-value.&lt;br /&gt;
&lt;br /&gt;
I hope this helps.--[[User:Able806|Able806]] 10:27, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:I’m still waiting to hear which literature says that “Monte Carlo resampling” is “more accurate than the chi-squared test”. The page mentioned above [http://faculty.vassar.edu/lowry/chi_beta.html] is a discussion of why statisticians “fail to reject the null” rather than “accepting the null” when the p-value is above 0.05 or so. The page says nothing about superiority of Monte Carlo methods. Why were alternate hypothesis distributions mentioned? Only the null hypothesis distribution is used to calculate a p-value. Yates’s correction is for 2x2 contingency tables [http://en.wikipedia.org/wiki/Yates%27_correction_for_continuity]. It doesn’t apply in this case. Finally, what the heck do “covariance structure analysis” and “allele frequencies at a highly polymorphic locus” have to do with this problem? [[User:SJohnson|SJohnson]] 16:38, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::SJohnson, I am looking for this paper for you, I cited it for one of my past publications dealing with allele frequencies (I believe it came from the Duke Biostatistics group).  To answer your question about allele frequencies, that is the issue at hand, more about the genetics than the math, but it is the item being studied.  So you stated that Yates can not be used and statistics says the number of occurrences is too small to evaluate using the Chi-Squared test so what would you recommend instead of the Monte-Carlo Method?&lt;br /&gt;
&lt;br /&gt;
:Regarding the &amp;quot;Fisher z-transformation p-value&amp;quot; from the paper, garbage in garbage out. If the p-values were bad to begin with, then why would a combination of them be meaningful? [[User:SJohnson|SJohnson]] 10:49, 9 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::You are assuming that p-values are wrong based on a test that is inappropriate in this case due to data limitations.  Did you perform a z-transformation on the chi-squared for the three data groups?--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
Quick question for SJohnson: How many degrees of freedom did you choose when calculating the p-value? I'd like to know upon what condition you base that number. Thanks.--[[User:Argon|Argon]] 11:05, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:The degree of freedom for a contingency table is rows minus one times columns minus one. That is, &amp;lt;math&amp;gt; (r-1)(c-1) &amp;lt;/math&amp;gt;. Here’s a pretty good tutorial I came across: [http://faculty.uncfsu.edu/dwallace/lesson%2020.pdf]. For the experiments from [http://www.pnas.org/content/105/23/7899.full.pdf], the DOFs are 11, 11, and 13. For experiment one, the chi-square test statistic is&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
X^2&lt;br /&gt;
=\sum\limits_i\sum\limits_j&lt;br /&gt;
\frac{\left(n_{i,j}-E\left[n_{i,j}\right]\right)^2}&lt;br /&gt;
{E\left[n_{i,j}\right]}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
=\frac{\left(0-1/3\right)^2}{1/3}&lt;br /&gt;
+\frac{\left(6-17/3\right)^2}{17/3}&lt;br /&gt;
+\frac{\left(0-1/3\right)^2}{1/3}&lt;br /&gt;
+\ldots+&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
+\frac{\left(2-1/3\right)^2}{1/3}&lt;br /&gt;
+\frac{\left(4-17/3\right)^2}{17/3}&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
\approx&lt;br /&gt;
14.82&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
:where &amp;lt;math&amp;gt;n_{i,j}&amp;lt;/math&amp;gt; is the observed value and &amp;lt;math&amp;gt;E\left[n_{i,j}\right]&amp;lt;/math&amp;gt; is the expected null hypothesis value. So if you have MS Excel, another way to arrive at the p-value of 0.19 is to type “=CHIDIST(14.82,11)” into a cell. Cheers! [[User:SJohnson|SJohnson]] 16:38, 5 March 2009 (EST)&lt;br /&gt;
::OK, thanks for the info. From what I'd calculated and looked up in tables, the numbers seemed close to a df=11 for a chi-square of ~14. (Aside: With terms having 17/3 in the denominator in the figures above, were you using the test of independence? I was using Pearson's test for [http://en.wikipedia.org/wiki/Pearson%27s_chi-square_test#Test_for_fit_of_a_distribution fit of a distribution] which returns a chi-squared value of 14 and roughly matched the p-values you reported, assuming the df was 11).&lt;br /&gt;
&lt;br /&gt;
::Also, the first sentence of the article reads: &amp;quot;Blount, Borland, and Lenski[1] claimed that a key evolutionary innovation was observed during a laboratory experiment. That claim is false.&amp;quot; A small correction: There were several claims in the paper. The 'key evolutionary innovation' was acquiring the ability to utilize citrate as a food source. That claim was demonstrated multiple times. The claim, which pertains to this statistics discussion was that the Cit+ phenotype arose in a multi-step process, first requiring a rare, pre-adaptive mutation before additional mutation(s) lead to the subsequent development of citrate utilization.--[[User:Argon|Argon]] 20:46, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:::My biology-degreed wife assures me that mutation does not necessarily mean that evolution occurred. What the paper claimed is that evolution (a “key innovation”) occurred in the lab. The key innovation supposedly increased the mutation rate. In the experiments, the observed mutation rate increased after generation 31,000, but not enough to make a statistically significant claim that the rate is not constant. The analysis in the paper was similar to flipping a coin ten times, counting six heads and claiming that the coin must be biased against tails. In reality, there’s nothing surprising about a fair coin producing slightly more of one outcome than the other. Just like there's nothing surprising about there being slightly more mutations in later generations than early generations given the null hypothesis (constant mutation rate). [[User:SJohnson|SJohnson]] 10:46, 9 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
::::SJohnson, not to say anything about your wife, but has she had a 400 level molecular genetics course (most general biology degrees do not cover the detail unless they are specialized)?  If so, she would have mentioned that if the mutation passes to the offspring and is selectively beneficial to the population then it is a step of evolution as along as the conditions continue through the sharing of the mutation with the population and the environment is such that reduces the growth rate of the non-transformed population.  While not all mutations are signs that evolution occurred the mutations that pass to offspring and provide a benefit compared to other offspring are very strong indicators.  In the case of this paper the population that evolved the cit+ was able to metabolize a chemical in their environment which allowed for an adaptation advantage compared to the non-transformed colonies.--[[User:Able806|Able806]] 10:19, 11 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
&lt;br /&gt;
Let’s go back to the beginning. There appears to be confusion about the difference between test statistics and methods for computing p-values. As is noted at the beginning of the page [http://www.conservapedia.com/Significance_of_E._Coli_Evolution_Experiments], the fundamental problem with the paper is that it used a flawed test statistic, not that it used Monte Carlo methods to find the p-value for that flawed statistic.&lt;br /&gt;
&lt;br /&gt;
Every hypothesis test uses a test statistic to reduce the data to a single number. The p-value for the test statistic can be calculated analytically (as I’ve done for the chi-square test statistic) or by Monte Carlo methods. In the paper, Monte Carlo methods were used to compute the p-value of the “mutation generation” test statistic. The key problem with the analysis from the paper is that it doesn’t work to use a weighted average to test for variations in mutation rate. This is like trying to use the sample variance to test for an increase in the mean in Gaussian-distributed data. A statistic should be selected based on the null and alternate hypothesis distributions of the data. The chi-square test (unlike the weighted average from the paper) is a reasonable choice for data that mutates at a constant rate under the null hypothesis, but mutates at varying rates under the alternate hypothesis.&lt;br /&gt;
&lt;br /&gt;
Able806, you made a good point about the contingency table cell frequencies being relatively low, but were wrong when you said ”the data set is actually too small to use the chi square method correctly”. In the low cell frequency case the chi-square test is still effective, but the null hypothesis distribution of the chi-square statistic starts to look less like the chi-square distribution. Thus, p-values calculated using the chi-square distribution may be a bit off. However, Monte Carlo p-values are always imperfect as well because it's impossible to generate an infinite number of random realizations. There are imperfections in p-values generated by analytic and Monte Carlo methods. However, low cell frequencies does not explain the &amp;gt;20x and &amp;gt;2.5x differences between chi-square p-values and p-values from the paper for experiments one and three. The reason for those huge differences was the use of the flawed test statistic (“mutation generation”) in the paper. [[User:SJohnson|SJohnson]] 16:38, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
== Misinterpretation of test ==&lt;br /&gt;
&lt;br /&gt;
SJohnson, Your analysis misinterprets the test. You say the null hypothesis is that this mutation cannot happen. They saw a mutation (4 mutations, in fact, in the data set you show) so the null hypothesis (as you state is) is disproved. That's perfectly straightforward.&lt;br /&gt;
&lt;br /&gt;
I don't know what the &amp;quot;mean mutation generation&amp;quot; test is but you're doing when you apply a chi-squared test to this dataset is to test if the mutations are evenly distributed throughout the generations. Your test says they are, so there's no strong evidence to suppose that mutations are likely to occur in one generation rather than another in the series of tests. Blount's test says thay aren't, so it's more likely that the mutation will occur later in the series of tests. I can't tell which test is right without knowing more about the test that Blount used.&lt;br /&gt;
&lt;br /&gt;
But that point (the foregoing paragraph) has no bearing at all on the null hypothesis, as you describe it. The mutation appeared, so that means the hypothesis that the mutation can't happen is disproved. Very simple. [[User:FredFerguson|FredFerguson]] 21:10, 8 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:I never said that “the null hypothesis is that this mutation cannot happen”. The chi-square test statistic I'm using wouldn’t be defined if the null hypothesis mutation rate was zero because the &amp;lt;math&amp;gt;E\left[n_{i,j}\right]&amp;lt;/math&amp;gt; term in the denominator of the statistic (see above equation) would be zero.&lt;br /&gt;
&lt;br /&gt;
:The test statistic from the paper is the average of the generation numbers of observed mutations. For experiment one this number is&lt;br /&gt;
::&amp;lt;math&amp;gt;&lt;br /&gt;
\frac{1}{4}\left(30500+31500+2\times32500\right)= 31750.&lt;br /&gt;
&amp;lt;/math&amp;gt;&lt;br /&gt;
:The same number is shown in Table 2 of the paper. [[User:SJohnson|SJohnson]] 10:46, 9 March 2009 (EDT)&lt;br /&gt;
&lt;br /&gt;
:: SJohnson, the way you're calculating the chi-squared statistic implies that you're testing the null hypothesis of a constant mutation rate over time against an alternative hypothesis of a mutation rate which varies over time. [[User:FredFerguson|FredFerguson]] 11:02, 9 March 2009 (EDT)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634997</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634997"/>
		<updated>2009-03-05T16:23:59Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
When Jenner introduced vaccination he knew nothing of the infectious agents that cause disease: it was not until late in the 19th century that Robert Kock proved that infectious diseases are caused by microorganisms, each one responsible for a particular disease, or pathology.  We now recognize four broad categories of disease-causing [[microorganism]]s, or [[pathogen]]s: these are [[virus]]es; [[bacteria]]; pathogenic [[fungi]]; and other relatively large and complex eukaryotic organisms collectively termed [[parasite]]s.&lt;br /&gt;
&lt;br /&gt;
==See Also==&lt;br /&gt;
[[Koch's postulates]]&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634994</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634994"/>
		<updated>2009-03-05T16:18:38Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* History */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
When Jenner introduced vaccination he knew nothing of the infectious agents that cause disease: it was not until late in the 19th century that Robert Kock proved that infectious diseases are caused by microorganisms, each one responsible for a particular disease, or pathology.  We now recognize four broad categories of disease-causing [[microorganism]]s, or [[pathogen]]s: these are [[virus]]es; [[bacteria]]; pathogenic [[fungi]]; and other relatively large and complex eukaryotic organisms collectively termed [[parasite]]s.&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634993</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634993"/>
		<updated>2009-03-05T16:18:26Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* History */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
When Jenner introduced vaccination he knew nothing of the infectious agents that cause disease: it was not until late in the 19th century that Robert Kock proved that infectious diseases are caused by microorganisms, each one responsible for a particular disease, or pathology.  We now recognize four broad categories of disease-causing [[microorganism]]s, or [[pathogen]]s: these are [[virus]]es; [[bacteria]]; pathogenic [[fungi]]; and oher relatively large and complex eukaryotic organisms collectively termed [[parasite]]s.&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634992</id>
		<title>Immunology</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Immunology&amp;diff=634992"/>
		<updated>2009-03-05T16:12:54Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;The study of '''Immunology''' deals with [[immune system]] function.  This includes:&lt;br /&gt;
&lt;br /&gt;
* T cells&lt;br /&gt;
* B cells&lt;br /&gt;
* Neutrophils&lt;br /&gt;
* Basophils&lt;br /&gt;
* Eosinophils&lt;br /&gt;
* Granulocytes&lt;br /&gt;
* Macrophages&lt;br /&gt;
* Monocytes&lt;br /&gt;
* Dendritic cells&lt;br /&gt;
* Natural killer cells&lt;br /&gt;
&lt;br /&gt;
==History==&lt;br /&gt;
Immunology is a relatively new science.  Its origin is usually attributed to Edward Jenner, who discovered in 1796 that cowpox, or vaccinia, induced protection against human [[smallpox]], an often fatal disease.  Jenner called his procedure vaccination, and this term is stilled used to describe the inoculation of healthy individuals with weakened or attenuated strains of disease-causing agents to provide protection from disease.  Although Jenner’s experiment was successful, it took almost two centuries for smallpox vaccination to become universal, an advance that enabled the World Health Organization to announce in 1979 that smallpox had been eradicated, arguably the greatest triumph of modern medicine.&lt;br /&gt;
&lt;br /&gt;
[[category:medicine]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=NADH&amp;diff=634983</id>
		<title>NADH</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=NADH&amp;diff=634983"/>
		<updated>2009-03-05T15:58:26Z</updated>

		<summary type="html">&lt;p&gt;Able806: New page: '''Nicotinamide adenine dinucleotide''' consists of two nucleotides: one nucleotide containing an adenine base, and the other containing nicotinamide, joined by their phosphate groups.  NA...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;'''Nicotinamide adenine dinucleotide''' consists of two nucleotides: one nucleotide containing an adenine base, and the other containing nicotinamide, joined by their phosphate groups.  NAD&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; (the abbreviated deprotonated form of NADH) is a coenzyme found in most cellular organisms.  The molecule is important in metabolic oxidation-reduction reactions due to its electron transfer capability of its two forms, NADH (reduced form) and NAD&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; (oxidized form).&lt;br /&gt;
&lt;br /&gt;
[[Category:Biochemistry]]&lt;br /&gt;
[[Category:Chemistry]]&lt;br /&gt;
[[Category:Molecular Biology]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Nicotinamide_adenine_dinucleotide&amp;diff=634981</id>
		<title>Nicotinamide adenine dinucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Nicotinamide_adenine_dinucleotide&amp;diff=634981"/>
		<updated>2009-03-05T15:48:25Z</updated>

		<summary type="html">&lt;p&gt;Able806: Redirecting to NADH&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;#REDIRECT [[NADH]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Ribose&amp;diff=634980</id>
		<title>Ribose</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Ribose&amp;diff=634980"/>
		<updated>2009-03-05T15:46:14Z</updated>

		<summary type="html">&lt;p&gt;Able806: New page: '''Ribose''' is a 5 carbon cyclic sugar found commonly in nature.  The phosphorylated form is often found as a subunit to ATP,  NADH and several other metabolic energy compounds.  ...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;'''Ribose''' is a 5 carbon cyclic sugar found commonly in nature.  The phosphorylated form is often found as a subunit to [[ATP]],  [[NADH]] and several other metabolic energy compounds.&lt;br /&gt;
&lt;br /&gt;
[[Category:Biochemistry]]&lt;br /&gt;
[[Category:Chemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Adenosine_triphosphate&amp;diff=634978</id>
		<title>Adenosine triphosphate</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Adenosine_triphosphate&amp;diff=634978"/>
		<updated>2009-03-05T15:38:06Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;'''Adenosine triphosphate (ATP)''' is an organic compound composed of the nitrogenous base [[adenine]], the sugar [[ribose]], and three [[phosphate]] groups arranged in tandem. ATP serves as the major energy source within the cell where it is used to drive a number of biological processes such as [[photosynthesis]], vesicle trafficking, ionic symporters/antiporters (e.g. Na+/K+ pump), muscle contraction, and protein synthesis. It is broken down by [[hydrolysis]] to yield [[adenosine diphosphate]] ([[ADP]]), inorganic phosphate, and energy. [[ADP]] can be further broken down to yield [[adenosine monophosphate]] ([[AMP]]), an additional phosphate ion, and more energy. When the phosphate group and energy are used to drive other reactions, such as the synthesis of [[uridine diphosphate]] ([[UDP]]), an [[RNA]] precursor, from [[uridine monophosphate]] ([[UMP]]), the pair of reactions are said to be coupled. New ATP can be generated by two distinct processes, [[substrate level phosphorylation]] and [[oxidative phosphorylation]]. The latter is the end point of [[cellular respiration]] via the oxidation of glucose.  &lt;br /&gt;
&lt;br /&gt;
Extracellularly, ATP has been found to act as a [[neurotransmitter]]. ATP receptors are widespread throughout the body. On its own it is known to have effects on the arteries, intestines, lungs, and bladder. It may also be released in tandem with other neurotransmitters.&lt;br /&gt;
&lt;br /&gt;
[[Image:Atp.gif|Adenosine Triphosphate (ATP, fully protonated)]]&lt;br /&gt;
&lt;br /&gt;
==Structure==&lt;br /&gt;
The structure of ATP has an ordered carbon compound as a backbone, but the part that is critical is the triphosphate moiety. Three phosphate groups are connected by oxygens to one another. There are also side oxygens connected to the phosphorous atoms. Under normal conditions in the body, each of these oxygens has a negative charge, the negative charges repel each other resulting in stored potential energy.&lt;br /&gt;
&lt;br /&gt;
==References==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Biochemistry]]&lt;br /&gt;
[[Category:Molecular Biology]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=634976</id>
		<title>Talk:Significance of E. Coli Evolution Experiments</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=634976"/>
		<updated>2009-03-05T15:29:43Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;SJohnson, your assessment, while good in the utilization of the chi-squared test is unfortunately incorrect.  The Monte Carlo resampling gives a more accurate p-value than the chi-squared.  You may research the literature (i.e. publications in statistical mathematics, many pubs actualy compare Monte Carlo vs Chi Squared) to discover that this method is commonly used in advance statistical work and how it is more accurate than the chi-squared test.--[[User:Able806|Able806]] 17:00, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:It doesn’t make sense to compare the chi-square test, which is a specific statistical hypothesis test, to Monte Carlo methods, which can be used for anything from fluid motion modeling to p-value computations. You can use Monte Carlo methods to compute the p-values of the chi-square test!&lt;br /&gt;
&lt;br /&gt;
:Monte Carlo methods involve the generation of random realizations. Your broad claim the Monte Carlo methods are “more accurate” than the chi-square test is obviously incorrect because the accuracy of Monte Carlo methods always depends on the number of random realizations generated. When p-values are small, Monte Carlo methods are notoriously inaccurate unless the number of realizations generated is enormous.&lt;br /&gt;
&lt;br /&gt;
:Which publications compare Monte Carlo to chi-square and show that the former is more accurate? Could you provide specific examples? Thanks.  [[User:SJohnson|SJohnson]] 18:50, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:In furtherance of SJohnson's remarks with respect to rarely occurring events, the use of the basic Monte Carlo method is plainly incorrect for modeling a rarely occurring event, as the Lenski paper did.  This has long been pointed out in [[Flaws in Richard Lenski Study]].  I know [[evolutionists]] will never admit a flaw in anything promoting their pet theory, but this (and other) flaws in that paper is undeniable.&lt;br /&gt;
&lt;br /&gt;
:Watch how evolutionists defended obvious errors in the Lenski paper, and then realize why the [[Piltdown Man]] fraud was taught for 40 years without evolutionists admitting it was a hoax.--[[User:Aschlafly|Andy Schlafly]] 09:55, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Andy, how exactly is the Monte Carlo method incorrect to use in this case?  I have seen it used in publications with much smaller datasets.--[[User:Able806|Able806]] 10:29, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
Sjohnson, I believe you just proved my point.  In the literature of mean and covariance structure analysis, non-central chi-square distribution is commonly used to describe the behavior of the likelihood ratio statistic under alternative hypothesis; it is widely believed that the non-central chi-square distribution is justified by statistical theory. Actually, when the null hypothesis is not trivially violated, the non-central chi-square distribution cannot describe the LR statistic well even when data are normally distributed and the sample size is large. Monte Carlo results compare the strength of the normal distribution against that of the non-central chi-square distribution.  In an association analysis comparing cases and controls with respect to allele frequencies at a highly polymorphic locus, a potential problem is that the conventional chi-squared test may not be valid for a large, sparse contingency table. Reliance on statistics with known asymptotic distribution is unnecessary, as Monte Carlo simulations can be performed to estimate the significance level of the test statistic.&lt;br /&gt;
&lt;br /&gt;
Here is a [http://faculty.vassar.edu/lowry/chi_beta.html  link] to a great page the provides an interactive example as to why the Chi Squared test would provide poor results compared to the Monte Carlo in relation to the Lenski data workup.  &lt;br /&gt;
&lt;br /&gt;
Something you may have overlooked was that the data set is actually too small to use the chi square method correctly.  It is often accepted that is any of the analyzed data falls under 10 for a particular cell of the data set then the Yates correction needs to be applied; unfortunately the Yates correction can over correct thus skewing the p-value.  Lenksi seemed to understand this by supporting his Monte Carlo p-value results with the Fisher z-transformation p-value.&lt;br /&gt;
&lt;br /&gt;
I hope this helps.--[[User:Able806|Able806]] 10:27, 5 March 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=634973</id>
		<title>Talk:Significance of E. Coli Evolution Experiments</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=634973"/>
		<updated>2009-03-05T15:27:10Z</updated>

		<summary type="html">&lt;p&gt;Able806: Reply to SJohnson&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;SJohnson, your assessment, while good in the utilization of the chi-squared test is unfortunately incorrect.  The Monte Carlo resampling gives a more accurate p-value than the chi-squared.  You may research the literature (i.e. publications in statistical mathematics, many pubs actualy compare Monte Carlo vs Chi Squared) to discover that this method is commonly used in advance statistical work and how it is more accurate than the chi-squared test.--[[User:Able806|Able806]] 17:00, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:It doesn’t make sense to compare the chi-square test, which is a specific statistical hypothesis test, to Monte Carlo methods, which can be used for anything from fluid motion modeling to p-value computations. You can use Monte Carlo methods to compute the p-values of the chi-square test!&lt;br /&gt;
&lt;br /&gt;
:Monte Carlo methods involve the generation of random realizations. Your broad claim the Monte Carlo methods are “more accurate” than the chi-square test is obviously incorrect because the accuracy of Monte Carlo methods always depends on the number of random realizations generated. When p-values are small, Monte Carlo methods are notoriously inaccurate unless the number of realizations generated is enormous.&lt;br /&gt;
&lt;br /&gt;
:Which publications compare Monte Carlo to chi-square and show that the former is more accurate? Could you provide specific examples? Thanks.  [[User:SJohnson|SJohnson]] 18:50, 4 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:In furtherance of SJohnson's remarks with respect to rarely occurring events, the use of the basic Monte Carlo method is plainly incorrect for modeling a rarely occurring event, as the Lenski paper did.  This has long been pointed out in [[Flaws in Richard Lenski Study]].  I know [[evolutionists]] will never admit a flaw in anything promoting their pet theory, but this (and other) flaws in that paper is undeniable.&lt;br /&gt;
&lt;br /&gt;
:Watch how evolutionists defended obvious errors in the Lenski paper, and then realize why the [[Piltdown Man]] fraud was taught for 40 years without evolutionists admitting it was a hoax.--[[User:Aschlafly|Andy Schlafly]] 09:55, 5 March 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
Sjohnson, I believe you just proved my point.  In the literature of mean and covariance structure analysis, non-central chi-square distribution is commonly used to describe the behavior of the likelihood ratio statistic under alternative hypothesis; it is widely believed that the non-central chi-square distribution is justified by statistical theory. Actually, when the null hypothesis is not trivially violated, the non-central chi-square distribution cannot describe the LR statistic well even when data are normally distributed and the sample size is large. Monte Carlo results compare the strength of the normal distribution against that of the non-central chi-square distribution.  In an association analysis comparing cases and controls with respect to allele frequencies at a highly polymorphic locus, a potential problem is that the conventional chi-squared test may not be valid for a large, sparse contingency table. Reliance on statistics with known asymptotic distribution is unnecessary, as Monte Carlo simulations can be performed to estimate the significance level of the test statistic.&lt;br /&gt;
&lt;br /&gt;
Here is a [http://faculty.vassar.edu/lowry/chi_beta.html  link] to a great page the provides an interactive example as to why the Chi Squared test would provide poor results compared to the Monte Carlo in relation to the Lenski data workup.  &lt;br /&gt;
&lt;br /&gt;
Something you may have overlooked was that the data set is actually too small to use the chi square method correctly.  It is often accepted that is any of the analyzed data falls under 10 for a particular cell of the data set then the Yates correction needs to be applied; unfortunately the Yates correction can over correct thus skewing the p-value.  Lenksi seemed to understand this by supporting his Monte Carlo p-value results with the Fisher z-transformation p-value.&lt;br /&gt;
&lt;br /&gt;
I hope this helps.--[[User:Able806|Able806]] 10:27, 5 March 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=634579</id>
		<title>Talk:Significance of E. Coli Evolution Experiments</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Significance_of_E._Coli_Evolution_Experiments&amp;diff=634579"/>
		<updated>2009-03-04T22:00:03Z</updated>

		<summary type="html">&lt;p&gt;Able806: New page: SJohnson, your assessment, while good in the utilization of the chi-squared test is unfortunately incorrect.  The Monte Carlo resampling gives a more accurate p-value than the chi-squared....&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;SJohnson, your assessment, while good in the utilization of the chi-squared test is unfortunately incorrect.  The Monte Carlo resampling gives a more accurate p-value than the chi-squared.  You may research the literature (i.e. publications in statistical mathematics, many pubs actualy compare Monte Carlo vs Chi Squared) to discover that this method is commonly used in advance statistical work and how it is more accurate than the chi-squared test.--[[User:Able806|Able806]] 17:00, 4 March 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Methodological_naturalism&amp;diff=631776</id>
		<title>Talk:Methodological naturalism</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Methodological_naturalism&amp;diff=631776"/>
		<updated>2009-02-26T16:27:46Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* New start */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Circular definition comes into play here:&lt;br /&gt;
&lt;br /&gt;
:Many scientists of faith nevertheless adopt naturalism in their studies. This is because there is simply no way for an experiment to investigate forces which by their nature cannot be investigated scientifically.&lt;br /&gt;
&lt;br /&gt;
The definition of [[scientific investigation]] is &amp;quot;study of the natural (material) world&amp;quot;. Science thus ''limits itself'' to investigation of the [[material world]]. By this definition, studying anything beyord the material world is &amp;quot;not scientific&amp;quot;. Therefore (by this definition), studying supernatural phenomena is not scientific, and any experiment which investigates the supernatural is not a scientific investigation.&lt;br /&gt;
&lt;br /&gt;
What then is the rationale for limiting investigation to the material world, i.e. natural phenomena. Is it because there is no way at all to study it? Or simply that we have defined &amp;quot;scientific investigation&amp;quot; as &amp;quot;study of the material world only&amp;quot;.&lt;br /&gt;
&lt;br /&gt;
This is like defining geography so that it is limited to [[physical geography]] and excluding human culture, trade, etc. So ''National Geographic]] has gone way beyond its bounds, if [[geography]] is limited only to physical aspects such as geology, ecology, wildlife, etc.&lt;br /&gt;
&lt;br /&gt;
It's really a confounding of method and scope. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 14:30, 13 July 2007 (EDT)&lt;br /&gt;
&lt;br /&gt;
:I don't believe it's possible to say that science limitis itself to the material world...  I mean, science is basically testing the testable.  So what you are saying is that science is limiting itself to what is possible...  It's not as though you can test the untestable.[[User:Raggs|Raggs]] 09:06, 19 March 2008 (EDT)&lt;br /&gt;
&lt;br /&gt;
::Your words simply perpetuate the confusion. Let me try again:&lt;br /&gt;
&lt;br /&gt;
::Liberals and conservatives agree (1) that science should test the testable and that (2) science properly limits itself to investigating the possible. Agreed? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 14:15, 19 March 2008 (EDT)&lt;br /&gt;
&lt;br /&gt;
==New start==&lt;br /&gt;
&lt;br /&gt;
I had to delete the article, because it simply did not make any sense. Moreover, it completely obscures the main thing that people want to know about science and naturalism: &lt;br /&gt;
&lt;br /&gt;
:Do scientists assume that the material world is all there is?&lt;br /&gt;
&lt;br /&gt;
Now, I've heard it said that &amp;quot;methodological naturalism&amp;quot; is only a self-imposed restriction. That scientists aren't really endorsing materialism but have chosen to look only for physical causes, when studying matters of [[physical science]]. &lt;br /&gt;
&lt;br /&gt;
However, the only context in which I've heard this term is in the [[origins debate]], where it's used as the chief pretext for dismissing [[intelligent design]]. Then it starts becoming [[intellectually dishonest]], by using [[circular reasoning]]. &lt;br /&gt;
&lt;br /&gt;
They say that ID can't be &amp;quot;scientific&amp;quot; because [[science]] only examines physical causes. But ID says that the decision to confine one's research and study to physical causes is itself the problem! --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 15:30, 13 April 2008 (EDT)&lt;br /&gt;
&lt;br /&gt;
Very interesting conclusion Ed.  I would not say that scientists assume that the material world is all there is, as many scientists are of different faiths.  I would, however, say that science is limited based on methods of detection.  As such it is hard to not study the physical scientifically when the detection methods that currently exist are only able to detect the physical.  For example, if I were to say that there is a sunflower in the middle of the room, you could verify this by looking in the room.  However, if I were to say there is an invisible sunflower in the room you would be limited to detecting it through means that would not require optics, such as displacement methods.  To go further if I were to say there is a mass less, invisible, non-field rendering sunflower in the room you would be unable to verify this based on the current detection methods available currently.  The reason why so many scientist say the ID is not scientific is that there is no way to currently detect and research their hypothesis (That life was intelligently designed by something).  The reason why evolution does not fall into this situation is based on the hypothesized mechanism of evolution, that mutation can cause the diversity.  ID is based on the designer somehow causing the diversity however the mechanism has yet to be explained as to how the designer caused the diversity.  The problem, and therefore the reason why science is not accepting of ID, is that we are currently seeing microevolution occur based on the mechanisms explained by evolution however the best explanation that IDists can give is that the designer had predesigned this to occur without providing a mechanism as to how we can detect the hand of the designer or as to how it was preprogrammed.--[[User:Able806|Able806]] 11:27, 26 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Codon&amp;diff=628024</id>
		<title>Codon</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Codon&amp;diff=628024"/>
		<updated>2009-02-20T14:14:29Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Amino acid codon codes */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''codon''' is three bases in a [[DNA]] or [[RNA]] sequence which specify a single [[amino acid]].&lt;br /&gt;
&lt;br /&gt;
==Amino acid codon codes==&lt;br /&gt;
{|class=&amp;quot;wikitable&amp;quot; style=&amp;quot;text-align:center&amp;quot;&lt;br /&gt;
|+&lt;br /&gt;
|-&lt;br /&gt;
! Amino Acid !! Single Letter Code !! DNA Codons&lt;br /&gt;
|-&lt;br /&gt;
| Isoleucine || I || ATT, ATC, ATA&lt;br /&gt;
|-&lt;br /&gt;
| Leucine || L || CTT, CTC, CTA, CTG, TTA, TTG&lt;br /&gt;
|-&lt;br /&gt;
| Valine || V || GTT, GTC, GTA, GTG&lt;br /&gt;
|-&lt;br /&gt;
| Phenylalanine || F || TTT, TTC&lt;br /&gt;
|-&lt;br /&gt;
| Methionine || M || ATG &lt;br /&gt;
|-&lt;br /&gt;
| Cysteine || C || TGT, TGC&lt;br /&gt;
|-&lt;br /&gt;
| Alanine || A || GCT, GCC, GCA, GCG&lt;br /&gt;
|-&lt;br /&gt;
| Glycine || G || GGT, GGC, GGA, GGG&lt;br /&gt;
|-&lt;br /&gt;
|  Proline || P || CCT, CCC, CCA, CCG&lt;br /&gt;
|-&lt;br /&gt;
| Threonine || T || ACT, ACC, ACA, ACG&lt;br /&gt;
|-&lt;br /&gt;
| Serine || S || TCT, TCC, TCA, TCG, AGT, AGC&lt;br /&gt;
|-&lt;br /&gt;
| Tyrosine || Y || TAT, TAC&lt;br /&gt;
|-&lt;br /&gt;
| Tryptophan || W || TGG&lt;br /&gt;
|-&lt;br /&gt;
| Glutamine || Q || CAA, CAG&lt;br /&gt;
|-&lt;br /&gt;
| Asparagine || N || AAT, AAC &lt;br /&gt;
|-&lt;br /&gt;
| Histidine || H || CAT, CAC&lt;br /&gt;
|-&lt;br /&gt;
| Glutamic acid || E || GAA, GAG&lt;br /&gt;
|-&lt;br /&gt;
| Aspartic acid || D || GAT, GAC&lt;br /&gt;
|-&lt;br /&gt;
| Lysine || K || AAA, AAG&lt;br /&gt;
|-&lt;br /&gt;
| Arginine || R || CGT, CGC, CGA, CGG, AGA, AGG&lt;br /&gt;
|-&lt;br /&gt;
| Start Codons || Start || ATG, rarely GTG&lt;br /&gt;
|-&lt;br /&gt;
| Stop Codons || Stop || TAA, TAG, TGA&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Codon&amp;diff=628022</id>
		<title>Codon</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Codon&amp;diff=628022"/>
		<updated>2009-02-20T14:12:32Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''codon''' is three bases in a [[DNA]] or [[RNA]] sequence which specify a single [[amino acid]].&lt;br /&gt;
&lt;br /&gt;
==Amino acid codon codes==&lt;br /&gt;
{|class=&amp;quot;wikitable&amp;quot; style=&amp;quot;text-align:center&amp;quot;&lt;br /&gt;
|+&lt;br /&gt;
|-&lt;br /&gt;
! Amino Acid !! Single Letter Code !! DNA Codons&lt;br /&gt;
|-&lt;br /&gt;
| Isoleucine || I || ATT, ATC, ATA&lt;br /&gt;
|-&lt;br /&gt;
| Leucine || L || CTT, CTC, CTA, CTG, TTA, TTG&lt;br /&gt;
|-&lt;br /&gt;
| Valine || V || GTT, GTC, GTA, GTG&lt;br /&gt;
|-&lt;br /&gt;
| Phenylalanine || F || TTT, TTC&lt;br /&gt;
|-&lt;br /&gt;
| Methionine || M || ATG &lt;br /&gt;
|-&lt;br /&gt;
| Cysteine || C || TGT, TGC&lt;br /&gt;
|-&lt;br /&gt;
| Alanine || A || GCT, GCC, GCA, GCG&lt;br /&gt;
|-&lt;br /&gt;
| Glycine || G || GGT, GGC, GGA, GGG&lt;br /&gt;
|-&lt;br /&gt;
|  Proline || P || CCT, CCC, CCA, CCG&lt;br /&gt;
|-&lt;br /&gt;
| Threonine || T || ACT, ACC, ACA, ACG&lt;br /&gt;
|-&lt;br /&gt;
| Serine || S || TCT, TCC, TCA, TCG, AGT, AGC&lt;br /&gt;
|-&lt;br /&gt;
| Tyrosine || Y || TAT, TAC&lt;br /&gt;
|-&lt;br /&gt;
| Tryptophan || W || TGG&lt;br /&gt;
|-&lt;br /&gt;
| Glutamine || Q || CAA, CAG&lt;br /&gt;
|-&lt;br /&gt;
| Asparagine || Q || AAT, AAC &lt;br /&gt;
|-&lt;br /&gt;
| Histidine || Q || CAT, CAC&lt;br /&gt;
|-&lt;br /&gt;
| Glutamic acid   || Q || GAA, GAG&lt;br /&gt;
|-&lt;br /&gt;
| Aspartic acid || Q || GAT, GAC&lt;br /&gt;
|-&lt;br /&gt;
| Lysine || Q || AAA, AAG&lt;br /&gt;
|-&lt;br /&gt;
| Arginine || Q || CGT, CGC, CGA, CGG, AGA, AGG&lt;br /&gt;
|-&lt;br /&gt;
| Start Codons || Start || ATG, rarely GTG&lt;br /&gt;
|-&lt;br /&gt;
| Stop Codons || Stop || TAA, TAG, TGA&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=626264</id>
		<title>Talk:Point mutation</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=626264"/>
		<updated>2009-02-17T20:33:15Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Genetic information (continued) */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Genetic Information==&lt;br /&gt;
Philip, I have to ask about this addition, point mutations do not add information to the genome.  Whereas they do not change the genome size they can change what is actually produced.  For example, the sentence &amp;quot;I love my cat&amp;quot; vs. &amp;quot;I love my hat&amp;quot;.  Both are of the same size however the information is different.  While this was a simple explanation it does apply to genomic expression.  Many proteins are duplicated on the genome, this actually allows for gene regulation.  Based on the promoters and regulatory proteins it is possible to have a point mutation in one of the duplicated sequences that changes the function of the protein expressed, thereby increasing the information (original protein and mutant now expressed) but not changing genomic size.  Unless you are equating genomic size with information.  It might help if I write about gene regulation sometime, most are not exposed to it in college since it is a very specific topic.--[[User:Able806|Able806]] 09:33, 4 February 2009 (EST)&lt;br /&gt;
:: Rather a late response, and pointless, given the merge, but I was primarily correcting the wording to what the reference was actually claiming.  [[User:Philip J. Rayment|Philip J. Rayment]] 09:41, 11 February 2009 (EST)&lt;br /&gt;
:::Thank you, I had guessed that after reading through the reference a bit.  Something I have to ask, the papers published by the ICR and such groups, are they available for scientific review?  I would like to research their position about genetic information particularly in relation to increase of information.  From what I know of molecular genetics and information molecules, the ability for information to be increased through mutation is possible and has been observed.  I would like to research the claims of ICR and such as to why they believe these examples fail.  If you could be of assistance with this I would greatly appreciate it.--[[User:Able806|Able806]] 10:33, 11 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::: Almost all such papers are ''available'' for anybody (scientists or otherwise) to &amp;quot;review&amp;quot; (read and comment on), as they have been published.  But is that what you are asking?  Are you asking about peer review?  Papers published in the ''Journal of Creation'' and the ''CRS Quarterly'' are peer-reviewed.  I don't know about ICR papers, but I suspect that ones published in ''Impact'' would be also.&lt;br /&gt;
::::: [http://creationontheweb.com/content/view/3012/ This page] list a number of layman's articles and technical papers which cover the [[information]] aspect in more detail.  Also, Werner Gitt's ''In the Beginning was Information'' is [http://www.sedin.org/propeng/informat.htm available online].&lt;br /&gt;
::::: [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
Thank you, Philip.  This does help.  I am looking for tech papers due to the description of the method used to gather the data.  I understand their position; I am trying to understand why they believe it to be impossible.  A quick example&lt;br /&gt;
:The old dog ran.&lt;br /&gt;
:The old doe ran.&lt;br /&gt;
The first example provides the relative age of the animal, the animal, and the action.&lt;br /&gt;
The second example provides the relative age of the animal, the animal, the action, and the gender of the animal.&lt;br /&gt;
No increase in letters and only one letter switched however more information is provided.&lt;br /&gt;
Now I know this is an overly simplified example but it is possible with codons.  I will give an example of a sequence as soon as I find my codons to AA matrix.--[[User:Able806|Able806]] 09:19, 13 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:in my experience people struggle with the concept of a substitution mutation increasing information. Duplication is much easier to understand. Try [http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=34156 this]. If you're still not getting through, you need to make sure the subject has an appropriate understanding of the definitions of information and new information. [[User:Alexkm|Alexkm]] 09:59, 13 February 2009 (EST)&lt;br /&gt;
:: See the start of the last page (p.31) of [http://creationontheweb.com/images/pdfs/tj/j21_3/j21_3_27-31.pdf this article].  [[User:Philip J. Rayment|Philip J. Rayment]] 00:38, 14 February 2009 (EST)&lt;br /&gt;
I have no problem with understanding the idea of information addition, what I am trying to understand is why those who have problems with the idea of mutation leading to new information have issue with it.  I want to know what experiments and calculations they have done to infer this.  Just saying it does not make it so.--[[User:Able806|Able806]] 15:18, 13 February 2009 (EST)&lt;br /&gt;
::: I'll give an expanded answer on this below.  [[User:Philip J. Rayment|Philip J. Rayment]] 00:38, 14 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
----&lt;br /&gt;
::::A good, information-increasing point mutation that comes to mind is the [https://content.nejm.org/cgi/content/extract/350/20/2096 LRP5 substitution], which &amp;quot;[enhances] skeletal mass without causing complications of osteopetrosis&amp;quot;. Some users may be confused by the term &amp;quot;High-Bone-Mass Disease&amp;quot;. If so, please see the medical definition of [http://www.mercksource.com/pp/us/cns/cns_hl_dorlands_split.jsp?pg=/ppdocs/us/common/dorlands/dorland/three/000030493.htm disease]. Some people are unwilling to open their minds to this being an instance of increased information. If that is the case, please proffer a definition of information in this context. [[User:MattL|MattL]] 10:48, 11 February 2009 (EST)&lt;br /&gt;
::::: Most claims of information-increasing mutations turn out to nothing of the sort, and the linked extract of this paper does not have enough information to say one way or the other in this case.  However, a mutation that merely changes the ''quantity'' of something (mass in this case) is likely ''not'' an information-increasing mutation, just like a cake recipe that has a &amp;quot;mutation&amp;quot; in the quantity of flour is not adding new ''information''.  [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
:::::: I would disagree; most gene regulation is done by concentrations of protein.  Therefore changing the amounts would change the expression.  A prime example would be the insulin receptor.  This transmembrane protein is activated by insulin and causes several things to occur within the cell, however the concentration of insulin determines the order of events therefore, change the concentration gets a different result.  {{unsigned|Able806}}&lt;br /&gt;
::::::: How different?  Anything actually ''new''?  [[User:Philip J. Rayment|Philip J. Rayment]] 00:38, 14 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Can you write some simple introductory material about the [[genome]], [[genome expression]], [[regulatory protein]]s, [[gene regulation]], and [[mutation]]? Nearly all of our readers need to know about the basics before they can learn about advanced topics such as [[point mutation]]. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 09:39, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Sure, let me check out what we have already and work with that, many of these topics do overlap.--[[User:Able806|Able806]] 09:57, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
After looking at[[Mutation]] I believe this article should be merged with it.  There is a section for Substitution mutations where point mutations would fall.  Ed, can I move the text over to the mutation article and you can delete this page?--[[User:Able806|Able806]] 10:06, 4 February 2009 (EST)&lt;br /&gt;
:How about you move the text over and then reduce this page to a redirect. Do you know how to do that? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:09, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
Sure.--[[User:Able806|Able806]] 10:10, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
I already added to mutation.--[[User:Able806|Able806]] 10:15, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Thanks, I see it now. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:30, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
== Genetic information (continued) ==&lt;br /&gt;
&lt;br /&gt;
Here I want to elaborate a bit on the various claims about genetic information.&lt;br /&gt;
&lt;br /&gt;
'''Could it occur, in principle?'''.&lt;br /&gt;
&lt;br /&gt;
Werner Gitt, who wrote ''In the Beginning was Information'', argues that information is a ''message'', and that a message requires a message sender.  He therefore argues that information ''cannot'' arise naturalistically.  Here he is obviously not talking about information of the form that was not intended as a message, such as the &amp;quot;information&amp;quot; we glean from astronomy about the composition of stars, for example.  Or the &amp;quot;information&amp;quot; that a particular site must have been inhabited gleaned from the stone tools found there.  Indeed, he is talking about ''coded'' information&amp;amp;mdash;information that is conveyed by means of arbitrary symbols.  That is, symbols that only have meaning to someone who already knows the code.  Alphabetic writing uses such arbitrary symbols.  This is clear from the fact that the same symbols can mean different things to different people (i.e. different languages using the same alphabet).  So in English, a &amp;quot;gift&amp;quot; is a present, whereas in German a &amp;quot;gift&amp;quot; is a poison (which concerns German postal staff handling parcels marked &amp;quot;gift&amp;quot;!).  DNA is such a coded information system.&lt;br /&gt;
&lt;br /&gt;
'''Does it occur in observation?'''.&lt;br /&gt;
&lt;br /&gt;
Lee Spetner, who wrote ''Not by Chance''[http://creationontheweb.com/content/view/773], says that information ''has not been observed'' to arise by chance, not that it ''can't''.&lt;br /&gt;
{{QuoteBox|All point mutations that have been studied on a molecular level turn out to reduce the genetic information and not increase it. &amp;lt;small&amp;gt;(Spetner, p. 138)&amp;lt;/small&amp;gt;}}&lt;br /&gt;
Note that this is not the negative argument &amp;quot;we haven't seen it so it doesn't occur&amp;quot;.  The argument is that &amp;quot;we have seen lots of mutations, and they all ''decrease'' the genetic information&amp;quot;.  That doesn't say that it's impossible.  It says that you're arguing from faith (or wishful thinking), not the evidence, if you want to argue that mutations increase genetic information.&lt;br /&gt;
&lt;br /&gt;
Realising that this is a powerful argument against evolution, evolutionists now make various claims that new information ''has'' arisen from mutations, and various claims about how it could in theory.  Both groups of claims have been answered by creationists, and I think it's fair to say that ''most'' such claims have been debunked.  For example, two of the arguments are that organisms acquire new genetic information from other organisms, and that they acquire new genetic information by means of gene duplication.  But both these arguments don't stand up to scrutiny.  Acquiring genetic information from other organisms explains nothing about where the genetic information came from in the first place.  It is ''existing'' genetic information, not ''new'' information.  And duplication is a second copy of ''existing'' information, not ''new'' information.  But of course then they go on to more sophisticated arguments.  Another very common argument is acquired resistance to antibiotics and the like, but most if not all of these turn out to be either an ''existing'' resistance that natural selection causes to become widespread in the population, or due to a ''loss'' of information.&lt;br /&gt;
&lt;br /&gt;
'''Would a few examples solve the problem?'''&lt;br /&gt;
&lt;br /&gt;
For microbe-to-man evolution to have occurred, a ''huge'' amount of new information would have had to be generated.  So supplying a handful of questionable examples, which is all that has been offered so far, hardly solves the problem.  And when Richard Dawkins was interviewed for a video, he was unable to supply ''any'' examples of new genetic information arising in nature.&lt;br /&gt;
&lt;br /&gt;
Indeed, a creationary biologist has told me that he doesn't totally rule out the possibility of the extremely rare trivial information-gaining mutation.  I've seen this alluded to in creationary literature, although I'm not sure that I've ever seen it said explicitly.  However, I gather that Michael Behe's ''The Edge of evolution'' (which I haven't read) covers this point.  See [http://creationontheweb.com/content/view/6207/#txtRef19 here] for a mini-review of Behe's book.&lt;br /&gt;
&lt;br /&gt;
John Sanford (''Genetic Entropy and the Mystery of the Genome''), writing mainly about human evolution, points out that a few examples wouldn't solve the problem anyway.&lt;br /&gt;
{{QuoteBox|We can, at best, wave our hands when we speculate about how selection might synthesize ''new'' information.  It is inherently hypothetical.  In a sense it becomes a philosophical question and is not really subject of scientific analysis.  Strong arguments can be made against mutation/selection creating new information, but theorists can always speculate to the contrary (it is very difficult to prove that something can never happen).  However I believe the &amp;quot;going down&amp;quot; aspect of the genome is subject to actual scientific analysis.  It is for this reason that I have focused on the issue of the degradation of information.  I believe that it is subject to concrete analysis.  Such analysis persuasively argues that ''net'' information must be declining.  If this is true, then even if it could be shown that there were specific cases where new information ''might'' be synthesized via mutation/selection, it would still be meaningless since such new information would promptly then begin to degenerate again.  The net direction would still be ''down'', and complex genomes could never have arisen spontaneously. &amp;lt;small&amp;gt;(Sanford, p. 105, his italics)&amp;lt;/small&amp;gt;}}&lt;br /&gt;
&lt;br /&gt;
[[User:Philip J. Rayment|Philip J. Rayment]] 02:32, 14 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Thank you, for your summary.  I will take some time out to read some of these recommendations.  I believe the issue at the base of all of this is the term '''information'''.  I do not know if the issue with this term is the fact that the encoded proteins are not just the result of the code from the DNA, thereby making the term '''information''' an oversimplification or if it is the inference of some needed form of result due to the order of the code.  I will write more on this at a later date, I am a bit behind this week.--[[User:Able806|Able806]] 15:33, 17 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=623398</id>
		<title>Talk:Point mutation</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=623398"/>
		<updated>2009-02-13T20:18:44Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Genetic Information==&lt;br /&gt;
Philip, I have to ask about this addition, point mutations do not add information to the genome.  Whereas they do not change the genome size they can change what is actually produced.  For example, the sentence &amp;quot;I love my cat&amp;quot; vs. &amp;quot;I love my hat&amp;quot;.  Both are of the same size however the information is different.  While this was a simple explanation it does apply to genomic expression.  Many proteins are duplicated on the genome, this actually allows for gene regulation.  Based on the promoters and regulatory proteins it is possible to have a point mutation in one of the duplicated sequences that changes the function of the protein expressed, thereby increasing the information (original protein and mutant now expressed) but not changing genomic size.  Unless you are equating genomic size with information.  It might help if I write about gene regulation sometime, most are not exposed to it in college since it is a very specific topic.--[[User:Able806|Able806]] 09:33, 4 February 2009 (EST)&lt;br /&gt;
:: Rather a late response, and pointless, given the merge, but I was primarily correcting the wording to what the reference was actually claiming.  [[User:Philip J. Rayment|Philip J. Rayment]] 09:41, 11 February 2009 (EST)&lt;br /&gt;
:::Thank you, I had guessed that after reading through the reference a bit.  Something I have to ask, the papers published by the ICR and such groups, are they available for scientific review?  I would like to research their position about genetic information particularly in relation to increase of information.  From what I know of molecular genetics and information molecules, the ability for information to be increased through mutation is possible and has been observed.  I would like to research the claims of ICR and such as to why they believe these examples fail.  If you could be of assistance with this I would greatly appreciate it.--[[User:Able806|Able806]] 10:33, 11 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::: Almost all such papers are ''available'' for anybody (scientists or otherwise) to &amp;quot;review&amp;quot; (read and comment on), as they have been published.  But is that what you are asking?  Are you asking about peer review?  Papers published in the ''Journal of Creation'' and the ''CRS Quarterly'' are peer-reviewed.  I don't know about ICR papers, but I suspect that ones published in ''Impact'' would be also.&lt;br /&gt;
::::: [http://creationontheweb.com/content/view/3012/ This page] list a number of layman's articles and technical papers which cover the [[information]] aspect in more detail.  Also, Werner Gitt's ''In the Beginning was Information'' is [http://www.sedin.org/propeng/informat.htm available online].&lt;br /&gt;
::::: [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
Thank you, Philip.  This does help.  I am looking for tech papers due to the description of the method used to gather the data.  I understand their position; I am trying to understand why they believe it to be impossible.  A quick example&lt;br /&gt;
:The old dog ran.&lt;br /&gt;
:The old doe ran.&lt;br /&gt;
The first example provides the relative age of the animal, the animal, and the action.&lt;br /&gt;
The second example provides the relative age of the animal, the animal, the action, and the gender of the animal.&lt;br /&gt;
No increase in letters and only one letter switched however more information is provided.&lt;br /&gt;
Now I know this is an overly simplified example but it is possible with codons.  I will give an example of a sequence as soon as I find my codons to AA matrix.--[[User:Able806|Able806]] 09:19, 13 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:in my experience people struggle with the concept of a substitution mutation increasing information. Duplication is much easier to understand. Try [http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=34156 this]. If you're still not getting through, you need to make sure the subject has an appropriate understanding of the definitions of information and new information. [[User:Alexkm|Alexkm]] 09:59, 13 February 2009 (EST)&lt;br /&gt;
I have no problem with understanding the idea of information addition, what I am trying to understand is why those who have problems with the idea of mutation leading to new information have issue with it.  I want to know what experiments and calculations they have done to infer this.  Just saying it does not make it so.--[[User:Able806|Able806]] 15:18, 13 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::A good, information-increasing point mutation that comes to mind is the [https://content.nejm.org/cgi/content/extract/350/20/2096 LRP5 substitution], which &amp;quot;[enhances] skeletal mass without causing complications of osteopetrosis&amp;quot;. Some users may be confused by the term &amp;quot;High-Bone-Mass Disease&amp;quot;. If so, please see the medical definition of [http://www.mercksource.com/pp/us/cns/cns_hl_dorlands_split.jsp?pg=/ppdocs/us/common/dorlands/dorland/three/000030493.htm disease]. Some people are unwilling to open their minds to this being an instance of increased information. If that is the case, please proffer a definition of information in this context. [[User:MattL|MattL]] 10:48, 11 February 2009 (EST)&lt;br /&gt;
::::: Most claims of information-increasing mutations turn out to nothing of the sort, and the linked extract of this paper does not have enough information to say one way or the other in this case.  However, a mutation that merely changes the ''quantity'' of something (mass in this case) is likely ''not'' an information-increasing mutation, just like a cake recipe that has a &amp;quot;mutation&amp;quot; in the quantity of flour is not adding new ''information''.  [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
I would disagree; most gene regulation is done by concentrations of protein.  Therefore changing the amounts would change the expression.  A prime example would be the insulin receptor.  This transmembrane protein is activated by insulin and causes several things to occur within the cell, however the concentration of insulin determines the order of events therefore, change the concentration gets a different result.&lt;br /&gt;
&lt;br /&gt;
:Can you write some simple introductory material about the [[genome]], [[genome expression]], [[regulatory protein]]s, [[gene regulation]], and [[mutation]]? Nearly all of our readers need to know about the basics before they can learn about advanced topics such as [[point mutation]]. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 09:39, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Sure, let me check out what we have already and work with that, many of these topics do overlap.--[[User:Able806|Able806]] 09:57, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
After looking at[[Mutation]] I believe this article should be merged with it.  There is a section for Substitution mutations where point mutations would fall.  Ed, can I move the text over to the mutation article and you can delete this page?--[[User:Able806|Able806]] 10:06, 4 February 2009 (EST)&lt;br /&gt;
:How about you move the text over and then reduce this page to a redirect. Do you know how to do that? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:09, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
Sure.--[[User:Able806|Able806]] 10:10, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
I already added to mutation.--[[User:Able806|Able806]] 10:15, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Thanks, I see it now. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:30, 4 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=623396</id>
		<title>Talk:Point mutation</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=623396"/>
		<updated>2009-02-13T20:15:27Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Genetic Information==&lt;br /&gt;
Philip, I have to ask about this addition, point mutations do not add information to the genome.  Whereas they do not change the genome size they can change what is actually produced.  For example, the sentence &amp;quot;I love my cat&amp;quot; vs. &amp;quot;I love my hat&amp;quot;.  Both are of the same size however the information is different.  While this was a simple explanation it does apply to genomic expression.  Many proteins are duplicated on the genome, this actually allows for gene regulation.  Based on the promoters and regulatory proteins it is possible to have a point mutation in one of the duplicated sequences that changes the function of the protein expressed, thereby increasing the information (original protein and mutant now expressed) but not changing genomic size.  Unless you are equating genomic size with information.  It might help if I write about gene regulation sometime, most are not exposed to it in college since it is a very specific topic.--[[User:Able806|Able806]] 09:33, 4 February 2009 (EST)&lt;br /&gt;
:: Rather a late response, and pointless, given the merge, but I was primarily correcting the wording to what the reference was actually claiming.  [[User:Philip J. Rayment|Philip J. Rayment]] 09:41, 11 February 2009 (EST)&lt;br /&gt;
:::Thank you, I had guessed that after reading through the reference a bit.  Something I have to ask, the papers published by the ICR and such groups, are they available for scientific review?  I would like to research their position about genetic information particularly in relation to increase of information.  From what I know of molecular genetics and information molecules, the ability for information to be increased through mutation is possible and has been observed.  I would like to research the claims of ICR and such as to why they believe these examples fail.  If you could be of assistance with this I would greatly appreciate it.--[[User:Able806|Able806]] 10:33, 11 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::: Almost all such papers are ''available'' for anybody (scientists or otherwise) to &amp;quot;review&amp;quot; (read and comment on), as they have been published.  But is that what you are asking?  Are you asking about peer review?  Papers published in the ''Journal of Creation'' and the ''CRS Quarterly'' are peer-reviewed.  I don't know about ICR papers, but I suspect that ones published in ''Impact'' would be also.&lt;br /&gt;
::::: [http://creationontheweb.com/content/view/3012/ This page] list a number of layman's articles and technical papers which cover the [[information]] aspect in more detail.  Also, Werner Gitt's ''In the Beginning was Information'' is [http://www.sedin.org/propeng/informat.htm available online].&lt;br /&gt;
::::: [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
Thank you, Philip.  This does help.  I am looking for tech papers due to the description of the method used to gather the data.  I understand their position; I am trying to understand why they believe it to be impossible.  A quick example&lt;br /&gt;
:The old dog ran.&lt;br /&gt;
:The old doe ran.&lt;br /&gt;
The first example provides the relative age of the animal, the animal, and the action.&lt;br /&gt;
The second example provides the relative age of the animal, the animal, the action, and the gender of the animal.&lt;br /&gt;
No increase in letters and only one letter switched however more information is provided.&lt;br /&gt;
Now I know this is an overly simplified example but it is possible with codons.  I will give an example of a sequence as soon as I find my codons to AA matrix.--[[User:Able806|Able806]] 09:19, 13 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
 :in my experience people struggle with the concept of a substitution mutation increasing information. Duplication is much easier to understand. Try [http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=34156 this]. If you're still not getting through, you need to make sure the subject has an appropriate understanding of the definitions of information and new information. [[User:Alexkm|Alexkm]] 09:59, 13 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
::::A good, information-increasing point mutation that comes to mind is the [https://content.nejm.org/cgi/content/extract/350/20/2096 LRP5 substitution], which &amp;quot;[enhances] skeletal mass without causing complications of osteopetrosis&amp;quot;. Some users may be confused by the term &amp;quot;High-Bone-Mass Disease&amp;quot;. If so, please see the medical definition of [http://www.mercksource.com/pp/us/cns/cns_hl_dorlands_split.jsp?pg=/ppdocs/us/common/dorlands/dorland/three/000030493.htm disease]. Some people are unwilling to open their minds to this being an instance of increased information. If that is the case, please proffer a definition of information in this context. [[User:MattL|MattL]] 10:48, 11 February 2009 (EST)&lt;br /&gt;
::::: Most claims of information-increasing mutations turn out to nothing of the sort, and the linked extract of this paper does not have enough information to say one way or the other in this case.  However, a mutation that merely changes the ''quantity'' of something (mass in this case) is likely ''not'' an information-increasing mutation, just like a cake recipe that has a &amp;quot;mutation&amp;quot; in the quantity of flour is not adding new ''information''.  [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
I would disagree; most gene regulation is done by concentrations of protein.  Therefore changing the amounts would change the expression.  A prime example would be the insulin receptor.  This transmembrane protein is activated by insulin and causes several things to occur within the cell, however the concentration of insulin determines the order of events therefore, change the concentration gets a different result.&lt;br /&gt;
&lt;br /&gt;
:Can you write some simple introductory material about the [[genome]], [[genome expression]], [[regulatory protein]]s, [[gene regulation]], and [[mutation]]? Nearly all of our readers need to know about the basics before they can learn about advanced topics such as [[point mutation]]. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 09:39, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Sure, let me check out what we have already and work with that, many of these topics do overlap.--[[User:Able806|Able806]] 09:57, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
After looking at[[Mutation]] I believe this article should be merged with it.  There is a section for Substitution mutations where point mutations would fall.  Ed, can I move the text over to the mutation article and you can delete this page?--[[User:Able806|Able806]] 10:06, 4 February 2009 (EST)&lt;br /&gt;
:How about you move the text over and then reduce this page to a redirect. Do you know how to do that? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:09, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
Sure.--[[User:Able806|Able806]] 10:10, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
I already added to mutation.--[[User:Able806|Able806]] 10:15, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Thanks, I see it now. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:30, 4 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=623274</id>
		<title>Talk:Point mutation</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=623274"/>
		<updated>2009-02-13T14:19:20Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Genetic Information */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Genetic Information==&lt;br /&gt;
Philip, I have to ask about this addition, point mutations do not add information to the genome.  Whereas they do not change the genome size they can change what is actually produced.  For example, the sentence &amp;quot;I love my cat&amp;quot; vs. &amp;quot;I love my hat&amp;quot;.  Both are of the same size however the information is different.  While this was a simple explanation it does apply to genomic expression.  Many proteins are duplicated on the genome, this actually allows for gene regulation.  Based on the promoters and regulatory proteins it is possible to have a point mutation in one of the duplicated sequences that changes the function of the protein expressed, thereby increasing the information (original protein and mutant now expressed) but not changing genomic size.  Unless you are equating genomic size with information.  It might help if I write about gene regulation sometime, most are not exposed to it in college since it is a very specific topic.--[[User:Able806|Able806]] 09:33, 4 February 2009 (EST)&lt;br /&gt;
:: Rather a late response, and pointless, given the merge, but I was primarily correcting the wording to what the reference was actually claiming.  [[User:Philip J. Rayment|Philip J. Rayment]] 09:41, 11 February 2009 (EST)&lt;br /&gt;
:::Thank you, I had guessed that after reading through the reference a bit.  Something I have to ask, the papers published by the ICR and such groups, are they available for scientific review?  I would like to research their position about genetic information particularly in relation to increase of information.  From what I know of molecular genetics and information molecules, the ability for information to be increased through mutation is possible and has been observed.  I would like to research the claims of ICR and such as to why they believe these examples fail.  If you could be of assistance with this I would greatly appreciate it.--[[User:Able806|Able806]] 10:33, 11 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::::: Almost all such papers are ''available'' for anybody (scientists or otherwise) to &amp;quot;review&amp;quot; (read and comment on), as they have been published.  But is that what you are asking?  Are you asking about peer review?  Papers published in the ''Journal of Creation'' and the ''CRS Quarterly'' are peer-reviewed.  I don't know about ICR papers, but I suspect that ones published in ''Impact'' would be also.&lt;br /&gt;
::::: [http://creationontheweb.com/content/view/3012/ This page] list a number of layman's articles and technical papers which cover the [[information]] aspect in more detail.  Also, Werner Gitt's ''In the Beginning was Information'' is [http://www.sedin.org/propeng/informat.htm available online].&lt;br /&gt;
::::: [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
Thank you, Philip.  This does help.  I am looking for tech papers due to the description of the method used to gather the data.  I understand their position; I am trying to understand why they believe it to be impossible.  A quick example&lt;br /&gt;
:The old dog ran.&lt;br /&gt;
:The old doe ran.&lt;br /&gt;
The first example provides the relative age of the animal, the animal, and the action.&lt;br /&gt;
The second example provides the relative age of the animal, the animal, the action, and the gender of the animal.&lt;br /&gt;
No increase in letters and only one letter switched however more information is provided.&lt;br /&gt;
Now I know this is an overly simplified example but it is possible with codons.  I will give an example of a sequence as soon as I find my codons to AA matrix.--[[User:Able806|Able806]] 09:19, 13 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
::::A good, information-increasing point mutation that comes to mind is the [https://content.nejm.org/cgi/content/extract/350/20/2096 LRP5 substitution], which &amp;quot;[enhances] skeletal mass without causing complications of osteopetrosis&amp;quot;. Some users may be confused by the term &amp;quot;High-Bone-Mass Disease&amp;quot;. If so, please see the medical definition of [http://www.mercksource.com/pp/us/cns/cns_hl_dorlands_split.jsp?pg=/ppdocs/us/common/dorlands/dorland/three/000030493.htm disease]. Some people are unwilling to open their minds to this being an instance of increased information. If that is the case, please proffer a definition of information in this context. [[User:MattL|MattL]] 10:48, 11 February 2009 (EST)&lt;br /&gt;
::::: Most claims of information-increasing mutations turn out to nothing of the sort, and the linked extract of this paper does not have enough information to say one way or the other in this case.  However, a mutation that merely changes the ''quantity'' of something (mass in this case) is likely ''not'' an information-increasing mutation, just like a cake recipe that has a &amp;quot;mutation&amp;quot; in the quantity of flour is not adding new ''information''.  [[User:Philip J. Rayment|Philip J. Rayment]] 21:08, 11 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Can you write some simple introductory material about the [[genome]], [[genome expression]], [[regulatory protein]]s, [[gene regulation]], and [[mutation]]? Nearly all of our readers need to know about the basics before they can learn about advanced topics such as [[point mutation]]. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 09:39, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Sure, let me check out what we have already and work with that, many of these topics do overlap.--[[User:Able806|Able806]] 09:57, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
After looking at[[Mutation]] I believe this article should be merged with it.  There is a section for Substitution mutations where point mutations would fall.  Ed, can I move the text over to the mutation article and you can delete this page?--[[User:Able806|Able806]] 10:06, 4 February 2009 (EST)&lt;br /&gt;
:How about you move the text over and then reduce this page to a redirect. Do you know how to do that? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:09, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
Sure.--[[User:Able806|Able806]] 10:10, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
I already added to mutation.--[[User:Able806|Able806]] 10:15, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Thanks, I see it now. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:30, 4 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=622023</id>
		<title>Talk:Point mutation</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Point_mutation&amp;diff=622023"/>
		<updated>2009-02-11T15:33:46Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Genetic Information==&lt;br /&gt;
Philip, I have to ask about this addition, point mutations do not add information to the genome.  Whereas they do not change the genome size they can change what is actually produced.  For example, the sentence &amp;quot;I love my cat&amp;quot; vs. &amp;quot;I love my hat&amp;quot;.  Both are of the same size however the information is different.  While this was a simple explanation it does apply to genomic expression.  Many proteins are duplicated on the genome, this actually allows for gene regulation.  Based on the promoters and regulatory proteins it is possible to have a point mutation in one of the duplicated sequences that changes the function of the protein expressed, thereby increasing the information (original protein and mutant now expressed) but not changing genomic size.  Unless you are equating genomic size with information.  It might help if I write about gene regulation sometime, most are not exposed to it in college since it is a very specific topic.--[[User:Able806|Able806]] 09:33, 4 February 2009 (EST)&lt;br /&gt;
:: Rather a late response, and pointless, given the merge, but I was primarily correcting the wording to what the reference was actually claiming.  [[User:Philip J. Rayment|Philip J. Rayment]] 09:41, 11 February 2009 (EST)&lt;br /&gt;
:::Thank you, I had guessed that after reading through the reference a bit.  Something I have to ask, the papers published by the ICR and such groups, are they available for scientific review?  I would like to research their position about genetic information particularly in relation to increase of information.  From what I know of molecular genetics and information molecules, the ability for information to be increased through mutation is possible and has been observed.  I would like to research the claims of ICR and such as to why they believe these examples fail.  If you could be of assistance with this I would greatly appreciate it.--[[User:Able806|Able806]] 10:33, 11 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Can you write some simple introductory material about the [[genome]], [[genome expression]], [[regulatory protein]]s, [[gene regulation]], and [[mutation]]? Nearly all of our readers need to know about the basics before they can learn about advanced topics such as [[point mutation]]. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 09:39, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Sure, let me check out what we have already and work with that, many of these topics do overlap.--[[User:Able806|Able806]] 09:57, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
After looking at[[Mutation]] I believe this article should be merged with it.  There is a section for Substitution mutations where point mutations would fall.  Ed, can I move the text over to the mutation article and you can delete this page?--[[User:Able806|Able806]] 10:06, 4 February 2009 (EST)&lt;br /&gt;
:How about you move the text over and then reduce this page to a redirect. Do you know how to do that? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:09, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
Sure.--[[User:Able806|Able806]] 10:10, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
I already added to mutation.--[[User:Able806|Able806]] 10:15, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Thanks, I see it now. --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:30, 4 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=619296</id>
		<title>Nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=619296"/>
		<updated>2009-02-04T21:56:08Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a  nitrogenous base (a pyrimidine or purine). The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In [[DNA]] base pairing, adenine pairs with thymine, and guanine pairs with cytosine, while in [[RNA]] adenine pairs with uracil.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nitrogenous bases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidine monophosphate (TMP), Thymidine diphosphate (TDP) or Thymidine triphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine monophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nitrogenous bases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=RNA_nucleotide&amp;diff=619295</id>
		<title>RNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=RNA_nucleotide&amp;diff=619295"/>
		<updated>2009-02-04T21:54:16Z</updated>

		<summary type="html">&lt;p&gt;Able806: Redirecting to Nucleotide&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;#REDIRECT [[Nucleotide]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=619294</id>
		<title>Nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=619294"/>
		<updated>2009-02-04T21:53:16Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Pyrimidine Nucleobases */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a  nucleobase (a pyrimidine or purine). The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In [[DNA]] base pairing, adenine pairs with thymine, and guanine pairs with cytosine, while in [[RNA]] adenine pairs with uracil.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nucleobases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidine monophosphate (TMP), Thymidine diphosphate (TDP) or Thymidine triphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine monophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nuclobases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:Nucleotide&amp;diff=619291</id>
		<title>Talk:Nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:Nucleotide&amp;diff=619291"/>
		<updated>2009-02-04T21:48:30Z</updated>

		<summary type="html">&lt;p&gt;Able806: Moving talk over&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Sugar==&lt;br /&gt;
Not sure if it would be a good idea to label it as a sugar.  I believe to many people would consider it to be the same stuff I sweeten my ceral with.  The ribose sugar is a pentose unlike sucrose which is made up of dextrose.  We could do an article on the actual molecule like we have for the phosphate.--[[User:Able806|Able806]] 10:28, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Well, of course. &amp;quot;[[Sugar]]&amp;quot; indicates sweeteners such as [[table sugar]] (i.e., [[sucrose]]). We need to have a list of common sugars; they all end in '''-ose''', right?&lt;br /&gt;
&lt;br /&gt;
:Perhaps a more general word than [[ribose]] (or that thing with the 2 and the dash) would be [[carbohydrate]]. After giving a simple definition in the intro, we can provide more specific detailed information in the body of the article. Can you help with this? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:33, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::I will see what I can come up with, I have to head to the lab for now.  I starches and cellulose are carbohydrates as well so it is a question of how close do we want to come to the actural molecule name.  I am fine with Ribose since it is difficult to confuse it with table sugar.  We can add to the ribose article or even work on a sugar article as a classification with in organic chemistry.--[[User:Able806|Able806]] 10:36, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Go to the lab. It was sweet working with you. ;-) --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 11:00, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Lol, thanks.  I will see what I can do to flesh out this page a bit.--[[User:Able806|Able806]] 15:43, 4 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619290</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619290"/>
		<updated>2009-02-04T21:47:34Z</updated>

		<summary type="html">&lt;p&gt;Able806: Redirecting to Nucleotide&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;#REDIRECT [[Nucleotide]]&lt;br /&gt;
A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a  nucleobase (a pyrimidine or purine). The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In [[DNA]] base pairing, adenine pairs with thymine, and guanine pairs with cytosine, while in [[RNA]] adenine pairs with uracil.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nucleobases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine emonophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nuclobases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=619289</id>
		<title>Nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Nucleotide&amp;diff=619289"/>
		<updated>2009-02-04T21:46:56Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a  nucleobase (a pyrimidine or purine). The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In [[DNA]] base pairing, adenine pairs with thymine, and guanine pairs with cytosine, while in [[RNA]] adenine pairs with uracil.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nucleobases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine emonophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nuclobases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619288</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619288"/>
		<updated>2009-02-04T21:44:03Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a  nucleobase (a pyrimidine or purine). The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In [[DNA]] base pairing, adenine pairs with thymine, and guanine pairs with cytosine, while in [[RNA]] adenine pairs with uracil.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nucleobases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine emonophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nuclobases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619286</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619286"/>
		<updated>2009-02-04T21:38:17Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine Nucleobases==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine emonophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nuclobases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619285</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619285"/>
		<updated>2009-02-04T21:37:50Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Purine nucleotides */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine nucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine emonophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine Nuclobases==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
Adenine is derived from the two-ring parent molecule purine. Adenine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with an additional amine attached to the six-carbon ring. The adenine nucleoside is called adenosine and lacks only a phosphate to form a nucleotide. Adenosine can be phosphorylated with phosphoric acid groups, creating Adenosine monophosphate (AMP), Adenosine diphosphate (ADP) or [[Adenosine triphosphate]] ([[ATP]]). &lt;br /&gt;
&lt;br /&gt;
===Guanine===&lt;br /&gt;
Guanine, a two-ring molecular structure, and is derived from the two-ring parent molecule purine. Guanine is comprised a six-carbon pyrimidine ring fused with a five-carbon imidazole ring with a carbonyl and amine attached to the six-carbon ring. Being unsaturated, the bicyclic molecule is planar. The guanine nucleoside is called guanosine and lacks only a phosphate to form a nucleotide. Guanosine can be phosphorylated with phosphoric acid groups, creating Guanosine monophosphate (GMP), Guanosine diphosphate (GDP) or Guanosine triphosphate (GTP).&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619279</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619279"/>
		<updated>2009-02-04T21:24:10Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Pyrimidine nucleotides */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine nucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase. Cytodine can be phosphorylated with phosphoric acid groups, creating Cytodine monophosphate (CMP), Cytodine diphosphate (CDP) or Cytodine triphosphate (CTP).&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia. Uridine can be phosphorylated with phosphoric acid groups, creating Uridine emonophosphate (UMP), Uridine diphosphate (UDP) or Uridine triphosphate (UTP).&lt;br /&gt;
&lt;br /&gt;
==Purine nucleotides==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
===Guanine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619278</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619278"/>
		<updated>2009-02-04T21:18:34Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine nucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia.&lt;br /&gt;
&lt;br /&gt;
==Purine nucleotides==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
===Guanine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619277</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619277"/>
		<updated>2009-02-04T21:17:28Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Uracil */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine ribonucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
Uracil is a pyrimidine nucleobase, a heterocyclic aromatic organic compound. Uracil is a planar, unsaturated compound that has the ability to absorb light.  Found in RNA, uracil base pairs with adenine through hydrogen bonding and is replaced by thymine in DNA. Uracil can base pair with any of the bases depending on how the molecule arranges itself on the helix, but readily pairs with adenine. Uracil can also bind with a ribose sugar to form a ribonucleoside, uridine. When a phosphate attaches to uridine, uridine 5'-monophosphate is produced.  Uracil also recycles itself to form nucleotides by undergoing a series of phophoribosyltransferase reactions. Degradation of uracil produces substrates, aspartate, carbon dioxide, and ammonia.&lt;br /&gt;
&lt;br /&gt;
==Purine ribonucleotides==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
===Guanine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619274</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619274"/>
		<updated>2009-02-04T21:13:21Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Thymine */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine ribonucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
&lt;br /&gt;
==Purine ribonucleotides==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
===Guanine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619273</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619273"/>
		<updated>2009-02-04T21:13:07Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Cytosine */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine ribonucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. &lt;br /&gt;
&lt;br /&gt;
Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
Cytosine is a pyrimidine derivative, with a heterocyclic, aromatic ring, and two substituents attached. Cytosine is inherently unstable, and can change into uracil (spontaneous deamination) which can lead to a [[Mutation|point mutation]] if not repaired by the DNA repair enzymes, such as uracil glycosylase. Cytosine can also be methylated into 5-methylcytosine by an enzyme called DNA methyltransferase&lt;br /&gt;
&lt;br /&gt;
===Uracil===&lt;br /&gt;
&lt;br /&gt;
==Purine ribonucleotides==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
===Guanine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619272</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619272"/>
		<updated>2009-02-04T21:09:29Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Thymine */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine ribonucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
Thymine is also known as 5-methyluracil.  As a pyrimidine nucleobase, thymine is a heterocyclic aromatic organic compound. Thymine may be derived by methylation of uracil at the fifth carbon. &lt;br /&gt;
&lt;br /&gt;
Thymine combined with deoxyribose creates the nucleoside deoxythymidine, which is also know as thymidine. Thymidine can be phosphorylated with phosphoric acid groups, creating Thymidinemonophosphate (TMP), Thymidinediphosphate (TDP) or Thymidinetriphosphate (TTP).&lt;br /&gt;
&lt;br /&gt;
===Cytosine===&lt;br /&gt;
===Uracil===&lt;br /&gt;
&lt;br /&gt;
==Purine ribonucleotides==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
===Guanine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619270</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619270"/>
		<updated>2009-02-04T20:56:36Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Purine ribonucleotides */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine ribonucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
===Cytosine===&lt;br /&gt;
===Uracil===&lt;br /&gt;
&lt;br /&gt;
==Purine ribonucleotides==&lt;br /&gt;
===Adenine=== &lt;br /&gt;
===Guanine===&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619269</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619269"/>
		<updated>2009-02-04T20:56:00Z</updated>

		<summary type="html">&lt;p&gt;Able806: /* Pyrimidine ribonucleotides */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine ribonucleotides==&lt;br /&gt;
===Thymine===&lt;br /&gt;
===Cytosine===&lt;br /&gt;
===Uracil===&lt;br /&gt;
&lt;br /&gt;
==Purine ribonucleotides==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619267</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619267"/>
		<updated>2009-02-04T20:53:20Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
==Pyrimidine ribonucleotides==&lt;br /&gt;
&lt;br /&gt;
==Purine ribonucleotides==&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619263</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619263"/>
		<updated>2009-02-04T20:51:36Z</updated>

		<summary type="html">&lt;p&gt;Able806: This article needs to be renamed to just nucleotide.  Ribose makes it RNA whereas  2'-deoxyribose makes it DNA.&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]] or  2'-deoxyribose, and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;br /&gt;
[[Category:Biochemistry]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619260</id>
		<title>DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=DNA_nucleotide&amp;diff=619260"/>
		<updated>2009-02-04T20:44:39Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;A '''DNA nucleotide''' is made of a [[phosphate]], a molecule of [[ribose]], and another molecule called a [[nitrogenous base]]. The initial letters of the base names that spell out the [[genetic code]]. &lt;br /&gt;
A, T, G, and C stand for the chemicals [[adenine]], [[thymine]], [[guanine]], and [[cytosine]], respectively. In base pairing, adenine always pairs with thymine, and guanine always pairs with cytosine.&lt;br /&gt;
&lt;br /&gt;
== Sources ==&lt;br /&gt;
*[http://www.blurtit.com/q145909.html What Is A DNA Nucleotide?]&lt;br /&gt;
*[http://www.genome.gov/glossary.cfm?key=base%20pair Courtesy: National Human Genome Research Institute]&lt;br /&gt;
&lt;br /&gt;
[[Category:Genetics]]&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
	<entry>
		<id>https://www.conservapedia.com/index.php?title=Talk:DNA_nucleotide&amp;diff=619259</id>
		<title>Talk:DNA nucleotide</title>
		<link rel="alternate" type="text/html" href="https://www.conservapedia.com/index.php?title=Talk:DNA_nucleotide&amp;diff=619259"/>
		<updated>2009-02-04T20:43:30Z</updated>

		<summary type="html">&lt;p&gt;Able806: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;==Sugar==&lt;br /&gt;
Not sure if it would be a good idea to label it as a sugar.  I believe to many people would consider it to be the same stuff I sweeten my ceral with.  The ribose sugar is a pentose unlike sucrose which is made up of dextrose.  We could do an article on the actual molecule like we have for the phosphate.--[[User:Able806|Able806]] 10:28, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Well, of course. &amp;quot;[[Sugar]]&amp;quot; indicates sweeteners such as [[table sugar]] (i.e., [[sucrose]]). We need to have a list of common sugars; they all end in '''-ose''', right?&lt;br /&gt;
&lt;br /&gt;
:Perhaps a more general word than [[ribose]] (or that thing with the 2 and the dash) would be [[carbohydrate]]. After giving a simple definition in the intro, we can provide more specific detailed information in the body of the article. Can you help with this? --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 10:33, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::I will see what I can come up with, I have to head to the lab for now.  I starches and cellulose are carbohydrates as well so it is a question of how close do we want to come to the actural molecule name.  I am fine with Ribose since it is difficult to confuse it with table sugar.  We can add to the ribose article or even work on a sugar article as a classification with in organic chemistry.--[[User:Able806|Able806]] 10:36, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
:Go to the lab. It was sweet working with you. ;-) --[[User:Ed Poor|Ed Poor]] &amp;lt;sup&amp;gt;[[User talk:Ed Poor|Talk]]&amp;lt;/sup&amp;gt; 11:00, 4 February 2009 (EST)&lt;br /&gt;
&lt;br /&gt;
::Lol, thanks.  I will see what I can do to flesh out this page a bit.--[[User:Able806|Able806]] 15:43, 4 February 2009 (EST)&lt;/div&gt;</summary>
		<author><name>Able806</name></author>
	</entry>
</feed>