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An association mapping framework to account for potential sex difference in genetic architectures

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dc.contributor.authorKang, Eun Yong-
dc.contributor.authorLee, Cue Hyunkyu-
dc.contributor.authorFurlotte, Nicholas A.-
dc.contributor.authorJoo, Jong Wha J.-
dc.contributor.authorKostem, Emrah-
dc.contributor.authorZaitlen, Noah-
dc.contributor.authorEskin, Eleazar-
dc.contributor.authorHan, Buhm-
dc.date.accessioned2023-04-25T07:32:21Z-
dc.date.available2023-04-25T07:32:21Z-
dc.date.created2018-12-27-
dc.date.created2018-12-27-
dc.date.created2018-12-27-
dc.date.issued2018-07-
dc.identifier.citationGenetics, Vol.209 No.3, pp.685-698-
dc.identifier.issn0016-6731-
dc.identifier.urihttps://hdl.handle.net/10371/191517-
dc.description.abstractOver the past few years, genome-wide association studies have identified many trait-associated loci that have different effects on females and males, which increased attention to the genetic architecture differences between the sexes. The between-sex differences in genetic architectures can cause a variety of phenomena such as differences in the effect sizes at trait-associated loci, differences in the magnitudes of polygenic background effects, and differences in the phenotypic variances. However, current association testing approaches for dealing with sex, such as including sex as a covariate, cannot fully account for these phenomena and can be suboptimal in statistical power. We present a novel association mapping framework, MetaSex, that can comprehensively account for the genetic architecture differences between the sexes. Through simulations and applications to real data, we show that our framework has superior performance than previous approaches in association mapping.-
dc.language영어-
dc.publisherGenetics Society of America-
dc.titleAn association mapping framework to account for potential sex difference in genetic architectures-
dc.typeArticle-
dc.identifier.doi10.1534/genetics.117.300501-
dc.citation.journaltitleGenetics-
dc.identifier.wosid000437171700005-
dc.identifier.scopusid2-s2.0-85049673073-
dc.citation.endpage698-
dc.citation.number3-
dc.citation.startpage685-
dc.citation.volume209-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorHan, Buhm-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusGENOME-WIDE ASSOCIATION-
dc.subject.keywordPlusMETAANALYSIS-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusPOPULATION-
dc.subject.keywordPlusCOHORT-
dc.subject.keywordPlusWOMEN-
dc.subject.keywordPlusMEN-
dc.subject.keywordAuthorAssociation Mapping-
dc.subject.keywordAuthorGenome-Wide Association Study-
dc.subject.keywordAuthorGenetics of Sex-
dc.subject.keywordAuthorLinear Mixed Model-
dc.subject.keywordAuthorMeta-Analysis-
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  • College of Medicine
  • Department of Medicine
Research Area Bioinformatics, Genomics, Statistical Genetics

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