17 Aug
2009
Researchers sequence exomes of 12 people
In a pioneering effort that generated massive amounts of DNA sequence data from 12 people, a team supported by the National Institutes of Health (NIH) has demonstrated the feasibility and value of a new strategy for identifying relatively rare genetic variants that may cause or contribute to disease. The proof-of-concept findings were published online today in the journal Nature.......
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Monday, August 17th, 2009 at 5:40 am under
