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PMID: 21169375 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Adjustment for local ancestry in genetic association analysis of admixed populations.

Bioinformatics (Oxford, England) ·Vol. 27 ·No. 5 ·2011-03-01 ·Pages 670-7

Wang X, Zhu X, Qin H, Cooper RS, Ewens WJ, Li C, Li M

Abstract

Admixed populations offer a unique opportunity for mapping diseases that have large disease allele frequency differences between ancestral populations. However, association analysis in such populations is challenging because population stratification may lead to association with loci unlinked to the disease locus. We show that local ancestry at a test single nucleotide polymorphism (SNP) may confound with the association signal and ignoring it can lead to spurious association. We demonstrate theoretically that adjustment for local ancestry at the test SNP is sufficient to remove the spurious association regardless of the mechanism of population stratification, whether due to local or global ancestry differences among study subjects; however, global ancestry adjustment procedures may not be effective. We further develop two novel association tests that adjust for local ancestry. Our first test is based on a conditional likelihood framework which models the distribution of the test SNP given disease status and flanking marker genotypes. A key advantage of this test lies in its ability to incorporate different directions of association in the ancestral populations. Our second test, which is computationally simpler, is based on logistic regression, with adjustment for local ancestry proportion. We conducted extensive simulations and found that the Type I error rates of our tests are under control; however, the global adjustment procedures yielded inflated Type I error rates when stratification is due to local ancestry difference.

MeSH Terms
Computer Simulation Gene Frequency Genetic Predisposition to Disease Genetics, Population/methods Genome-Wide Association Study/methods Genotype Humans Likelihood Functions Logistic Models Polymorphism, Single Nucleotide
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Wang Xuexia
Department of Biostatistics and Epidemiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Zhu Xiaofeng
Qin Huaizhen
Cooper Richard S
Ewens Warren J
Li Chun
Li Mingyao
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Article Info
Journal
Bioinformatics (Oxford, England)
Abbr.
Bioinformatics
ISSN
1367-4811
Published
2011-03-01
Epub
2010-00-17
Pages
670-7
Language
English
Region
England
NLM ID
9808944
PMCID
PMC3042179
Subset
IM
Grants
NHGRI NIH HHS · R01 HG003054 · United States
NHGRI NIH HHS · R01HG005854 · United States
NHLBI NIH HHS · R01 HL074166 · United States
NHGRI NIH HHS · R01 HG004517 · United States
NHLBI NIH HHS · R01HL074166 · United States
NHGRI NIH HHS · R01 HG005854 · United States
NHGRI NIH HHS · R01HG004517 · United States
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