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Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies

dc.contributor.authorGuan, Weihuaen_US
dc.contributor.authorLiang, Limingen_US
dc.contributor.authorBoehnke, Michaelen_US
dc.contributor.authorAbecasis, Gonçalo R.en_US
dc.date.accessioned2009-09-02T14:38:18Z
dc.date.available2010-10-05T18:27:29Zen_US
dc.date.issued2009-09en_US
dc.identifier.citationGuan, Weihua; Liang, Liming; Boehnke, Michael; Abecasis, GonÇalo R. (2009). "Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies." Genetic Epidemiology 33(6): 508-517. <http://hdl.handle.net/2027.42/63598>en_US
dc.identifier.issn0741-0395en_US
dc.identifier.issn1098-2272en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/63598
dc.description.abstractGenome-wide association studies are helping to dissect the etiology of complex diseases. Although case-control association tests are generally more powerful than family-based association tests, population stratification can lead to spurious disease-marker association or mask a true association. Several methods have been proposed to match cases and controls prior to genotyping, using family information or epidemiological data, or using genotype data for a modest number of genetic markers. Here, we describe a genetic similarity score matching (GSM) method for efficient matched analysis of cases and controls in a genome-wide or large-scale candidate gene association study. GSM comprises three steps: (1) calculating similarity scores for pairs of individuals using the genotype data; (2) matching sets of cases and controls based on the similarity scores so that matched cases and controls have similar genetic background; and (3) using conditional logistic regression to perform association tests. Through computer simulation we show that GSM correctly controls false-positive rates and improves power to detect true disease predisposing variants. We compare GSM to genomic control using computer simulations, and find improved power using GSM. We suggest that initial matching of cases and controls prior to genotyping combined with careful re-matching after genotyping is a method of choice for genome-wide association studies. Genet. Epidemiol . 33:508–517, 2009. © 2009 Wiley-Liss, Inc.en_US
dc.format.extent322577 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherGeneticsen_US
dc.titleGenotype-based matching to correct for population stratification in large-scale case-control genetic association studiesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, Michigan ; These authors contributed equally to this work.en_US
dc.contributor.affiliationumDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, Michigan ; Department of Biostatistics, School of Public Health, University of Michigan, 1420 Washington Heights, Ann Arbor MI 48109-2029en_US
dc.identifier.pmid19170134en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/63598/1/20403_ftp.pdf
dc.identifier.doi10.1002/gepi.20403en_US
dc.identifier.sourceGenetic Epidemiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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