4.5 Article

Discerning the ancestry of European Americans in genetic association studies

期刊

PLOS GENETICS
卷 4, 期 1, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.0030236

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资金

  1. NCRR NIH HHS [U54 RR020278] Funding Source: Medline
  2. NHGRI NIH HHS [U01 HG004168] Funding Source: Medline
  3. NIMH NIH HHS [MH 63420, R01 MH060870, R01 MH067257, R01 MH059586, MH067257, R01 MH059587, MH059588, R01 MH059566, MH59566, MH59587, R01 MH061675, MH061675, MH60870, MH59586, R01 MH059571, R01 MH060879, R01 MH059565, MH059571, U01 MH060879, MH059565, R01 MH063420, R01 MH059588] Funding Source: Medline
  4. NATIONAL CENTER FOR RESEARCH RESOURCES [U54RR020278] Funding Source: NIH RePORTER
  5. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [U01HG004168] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH060870, R01MH059566, R01MH060879, R01MH067257, R01MH059565, R01MH059586, R01MH059571, R01MH059588, R01MH061675, R01MH059587, R01MH063420] Funding Source: NIH RePORTER

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European Americans are often treated as a homogeneous group, but in fact form a structured population due to historical immigration of diverse source populations. Discerning the ancestry of European Americans genotyped in association studies is important in order to prevent false-positive or false-negative associations due to population stratification and to identify genetic variants whose contribution to disease risk differs across European ancestries. Here, we investigate empirical patterns of population structure in European Americans, analyzing 4,198 samples from four genome-wide association studies to show that components roughly corresponding to northwest European, southeast European, and Ashkenazi Jewish ancestry are the main sources of European American population structure. Building on this insight, we constructed a panel of 300 validated markers that are highly informative for distinguishing these ancestries. We demonstrate that this panel of markers can be used to correct for stratification in association studies that do not generate dense genotype data.

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