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