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Integrating common and rare genetic variation in diverse human populations.

Abstract:

Despite great progress in identifying genetic variants that influence human disease, most inherited risk remains unexplained. A more complete understanding requires genome-wide studies that fully examine less common alleles in populations with a wide range of ancestry. To inform the design and interpretation of such studies, we genotyped 1.6 million common single nucleotide polymorphisms (SNPs) in 1,184 reference individuals from 11 global populations, and sequenced ten 100-kilobase regions i...

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Publication status:
Published

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Publisher copy:
10.1038/nature09298

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Journal:
Nature
Volume:
467
Issue:
7311
Pages:
52-58
Publication date:
2010-09-01
DOI:
EISSN:
1476-4687
ISSN:
0028-0836
Source identifiers:
71238
Language:
English
Keywords:
Pubs id:
pubs:71238
UUID:
uuid:5c8c7a65-5fca-45db-bbcb-53ce0ebf84df
Local pid:
pubs:71238
Deposit date:
2012-12-19

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