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	<title>Comments on: Genomic noise and individual variation</title>
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	<link>http://www.gnxp.com/new/2008/01/26/genomic-noise-and-individual-variation/</link>
	<description>Genetics</description>
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		<title>By: Luke Lea</title>
		<link>http://www.gnxp.com/new/2008/01/26/genomic-noise-and-individual-variation/#comment-9452</link>
		<dc:creator><![CDATA[Luke Lea]]></dc:creator>
		<pubDate>Mon, 28 Jan 2008 18:30:17 +0000</pubDate>
		<guid isPermaLink="false">#comment-9452</guid>
		<description><![CDATA[So Charles Murray&#039;s point (in the Bell Curve I think) that if we remove all environmental differences, then all the remaining differences would be genetic, is false?]]></description>
		<content:encoded><![CDATA[<p>So Charles Murray&#8217;s point (in the Bell Curve I think) that if we remove all environmental differences, then all the remaining differences would be genetic, is false?</p>
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		<title>By: omnivore</title>
		<link>http://www.gnxp.com/new/2008/01/26/genomic-noise-and-individual-variation/#comment-9453</link>
		<dc:creator><![CDATA[omnivore]]></dc:creator>
		<pubDate>Sat, 26 Jan 2008 21:05:12 +0000</pubDate>
		<guid isPermaLink="false">#comment-9453</guid>
		<description><![CDATA[I am very sympathetic to the noise argument.  In discussions of the proportion of variance explained in [important variable X], the statement that Y explains 40% of the variance is, in my experience, frequently greeted with the automatic assumption that some more-important causal factor must explain the remaining 60%.  Instead, the first question should be what proportion of the variance is explainable at all.  If 50% is due to noise, then 40% actually covers 80% of the explainable variance.&#160;&lt;br&gt;&#160;&lt;br&gt;Note that estimating the proportion of explainable variance is difficult, often (seemingly) impossible.  Reliability coefficients are useless, because variance also arises from non-identity between the measurement and the construct being measured.  If one can account for 100% of the variance, that&#039;s the end of the story, but one must not be working in population genetics.  A more typical situation is to have factors that cover a minority of the variance.  Then...what?  I wonder whether a principled way to decide between noise and as-yet-undetected causal factors exists, even in some useful subset of situations.]]></description>
		<content:encoded><![CDATA[<p>I am very sympathetic to the noise argument.  In discussions of the proportion of variance explained in [important variable X], the statement that Y explains 40% of the variance is, in my experience, frequently greeted with the automatic assumption that some more-important causal factor must explain the remaining 60%.  Instead, the first question should be what proportion of the variance is explainable at all.  If 50% is due to noise, then 40% actually covers 80% of the explainable variance.&nbsp;<br />&nbsp;<br />Note that estimating the proportion of explainable variance is difficult, often (seemingly) impossible.  Reliability coefficients are useless, because variance also arises from non-identity between the measurement and the construct being measured.  If one can account for 100% of the variance, that&#8217;s the end of the story, but one must not be working in population genetics.  A more typical situation is to have factors that cover a minority of the variance.  Then&#8230;what?  I wonder whether a principled way to decide between noise and as-yet-undetected causal factors exists, even in some useful subset of situations.</p>
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		<title>By: Jon Claerbout</title>
		<link>http://www.gnxp.com/new/2008/01/26/genomic-noise-and-individual-variation/#comment-9454</link>
		<dc:creator><![CDATA[Jon Claerbout]]></dc:creator>
		<pubDate>Sat, 26 Jan 2008 17:37:38 +0000</pubDate>
		<guid isPermaLink="false">#comment-9454</guid>
		<description><![CDATA[&lt;i&gt;the error term must includes simple stochastic noise on any part of the complex mapping from genotype to phenotype&lt;/i&gt;&#160;&lt;br&gt;&#160;&lt;br&gt;I see it a little differently.                                                                                                                                                                        &#160;&lt;br&gt;Let&#039;s talk about IQ.   It&#039;s variation could be regressed against a sum of parental IQ and SES (Socio-Econ-Standard).  What better environmental model do you have besides SES?  Maybe none, and that one is not measured very precisely.  You end up with a big residual even after doing your best to model both the genes and the environment.  As I&#039;m a seismologist I can only guess at the numbers, so I&#039;ll stop there.  The point is, there are lots of sources for errors besides in the gene--&gt;phen transform]]></description>
		<content:encoded><![CDATA[<p><i>the error term must includes simple stochastic noise on any part of the complex mapping from genotype to phenotype</i>&nbsp;<br />&nbsp;<br />I see it a little differently.                                                                                                                                                                        &nbsp;<br />Let&#8217;s talk about IQ.   It&#8217;s variation could be regressed against a sum of parental IQ and SES (Socio-Econ-Standard).  What better environmental model do you have besides SES?  Maybe none, and that one is not measured very precisely.  You end up with a big residual even after doing your best to model both the genes and the environment.  As I&#8217;m a seismologist I can only guess at the numbers, so I&#8217;ll stop there.  The point is, there are lots of sources for errors besides in the gene&#8211;&gt;phen transform</p>
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		<title>By: Daniel Newby</title>
		<link>http://www.gnxp.com/new/2008/01/26/genomic-noise-and-individual-variation/#comment-9455</link>
		<dc:creator><![CDATA[Daniel Newby]]></dc:creator>
		<pubDate>Sat, 26 Jan 2008 14:01:33 +0000</pubDate>
		<guid isPermaLink="false">#comment-9455</guid>
		<description><![CDATA[&lt;a href=&quot;http://www.ncbi.nlm.nih.gov/pubmed/17889509?ordinalpos=5&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&quot;&gt;This research&lt;/a&gt; found that 0.9% of cells in schizophrenic human brains are aneuploid for chromosome 1, whereas only 0.3% were in normal controls.  (Aneuploid == gain or loss of a chromosome.)]]></description>
		<content:encoded><![CDATA[<p><a href="http://www.ncbi.nlm.nih.gov/pubmed/17889509?ordinalpos=5&amp;itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum">This research</a> found that 0.9% of cells in schizophrenic human brains are aneuploid for chromosome 1, whereas only 0.3% were in normal controls.  (Aneuploid == gain or loss of a chromosome.)</p>
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