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<title>Medical Xpress: PHYSorg news tagged with: statistical genetics</title>
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     <title>Harmful protein-coding mutations in people arose largely in the past 5,000 to 10,000 years (Update)</title>
   	 <description>(Medical Xpress)—A study dating the age of more than 1 million single-letter variations in the human DNA code reveals that most of these mutations are of recent origin, evolutionarily speaking. These kinds of mutations change one nucleotide – an A, C, T or G – in the DNA sequence.  Over 86 percent of the harmful protein-coding mutations of this type arose in humans just during the past 5,000 to 10,000 years.</description>
	  <link>http://medicalxpress.com/news/2012-11-genetic-variation-varies-populations.html</link>
	 <category>Genetics</category>
	 <pubDate>Wed, 28 Nov 2012 13:00:37 EST</pubDate>
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     <title>Novel type 2 diabetes genetic study involves five major ancestry groups</title>
   	 <description>A consortium of scientists who are taking a novel approach in their research to detect the genetic variations that predispose individuals to type 2 diabetes provided an update of their findings at the American Society of Human Genetics (ASHG) 2012 meeting.</description>
	  <link>http://medicalxpress.com/news/2012-11-diabetes-genetic-involves-major-ancestry.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 08 Nov 2012 19:30:02 EST</pubDate>
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     <title>Surprising findings from Exome Sequencing Project reported</title>
   	 <description>A multi-institutional team of researchers has sequenced the DNA of 6,700 exomes, the portion of the genome that contains protein-coding genes, as part of the National Heart, Lung and Blood Institute (NHLBI)-funded Exome Sequencing Project, one of the largest medical sequencing studies ever undertaken.</description>
	  <link>http://medicalxpress.com/news/2012-11-exome-sequencing.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 06 Nov 2012 08:27:56 EST</pubDate>
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