2018GeneticsOpen access

An Association Mapping Framework To Account for Potential Sex Difference in Genetic Architectures

Eun Yong Kang, Cue Hyunkyu Lee, Nicholas A. Furlotte, Jong Wha J. Joo, Emrah Kostem, Noah Zaitlen, Eleazar Eskin, Buhm Han

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Abstract

Abstract Recent genome-wide association studies suggest that the human genetic architecture of complex traits may vary between males and females; however, traditional approaches for association mapping cannot fully account for these between-sex differences... Over 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.

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Abstract Recent genome-wide association studies suggest that the human genetic architecture of complex traits may vary between males and females; however, traditional approaches for association mapping cannot fully account for these between-sex differences... Over 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.

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Available abstract

Abstract Recent genome-wide association studies suggest that the human genetic architecture of complex traits may vary between males and females; however, traditional approaches for association mapping cannot fully account for these between-sex differences... Over 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.

Key concepts: Genetic architecture, Biology, Genetic association, Genome-wide association study, Association mapping, Association (psychology), Covariate, Trait

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