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	<title>Li2010 - Revision history</title>
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	<updated>2026-04-10T20:12:37Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://www.popgen.dk/angsd/index.php?title=Li2010&amp;diff=71&amp;oldid=prev</id>
		<title>Albrecht: Created page with &quot;Li Y, Vinckenbosch N, Tian G, Huerta-Sanchez E, Jiang T, Jiang H, Albrechtsen A, Andersen G, Cao H, Korneliussen T, et al., 2010. Resequencing of 200 human exomes identifies a...&quot;</title>
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		<updated>2012-06-14T19:40:28Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;Li Y, Vinckenbosch N, Tian G, Huerta-Sanchez E, Jiang T, Jiang H, Albrechtsen A, Andersen G, Cao H, Korneliussen T, et al., 2010. Resequencing of 200 human exomes identifies a...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Li Y, Vinckenbosch N, Tian G, Huerta-Sanchez E, Jiang T, Jiang H, Albrechtsen A, Andersen G, Cao H, Korneliussen T, et al., 2010. Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants. Nat Genet 42:969–972.&lt;/div&gt;</summary>
		<author><name>Albrecht</name></author>
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