Ziang Zhang, Jerald F Lawless, Andrew D Paterson, Lei Sun
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引用次数: 0
摘要
在全基因组关联研究(GWAS)中,通常需要测试单核苷酸多态性(snp, G’s)和环境变量(E’s)之间的相互作用,例如基因-环境(G x E)或基因-基因(G x G)相互作用。然而,直接考虑相互作用往往是不可行的,因为相互作用变量是潜在的或计算负担太大。对于近似正态分布的数量性状(Y),可以通过检验基因型间Y的异方差来间接检验GxE。然而,当性状是二元的时候,现有的基于检验性状跨基因型异方差的方法不能推广。在本文中,我们提出了一种间接测试二元性状互作效应的方法,并随后提出了一个联合测试,以解释GWAS期间每个SNP的主效应和互作效应。最后一种方法在实践中很容易实现——它只需要将一个非加性(即优势)项添加到标准的GWAS二元特征加性模型中,并测试其显著性。我们通过广泛的数值研究说明了该方法的统计特征,包括i型误差控制和功率。将我们的方法应用于英国生物银行数据集,我们展示了所提出方法的实际效用,揭示了具有潜在相互作用效应的强大潜力的snp和基因。
Detecting latent interaction effects when analyzing binary traits.
In genome-wide association studies (GWAS), it is often desirable to test for interactions, such as gene-environment (G x E) or gene-gene (G x G) interactions, between single-nucleotide polymorphisms (SNPs, G's) and environmental variables (E's). However, directly accounting for interaction is often infeasible, because the interacting variable is latent or the computational burden is too large. For quantitative traits (Y) that are approximately normally distributed, it has been shown that indirect testing on GxE can be done by testing for heteroskedasticity of Y between genotypes. However, when traits are binary, the existing methodology based on testing the heteroskedasticity of the trait across genotypes cannot be generalized. In this paper, we propose an approach to indirectly test interaction effects for binary traits and subsequently propose a joint test that accounts for the main and interaction effects of each SNP during GWAS. The final method is straightforward to implement in practice-it simply involves adding a non-additive (i.e., dominance) term to standard GWAS additive models for binary traits and testing its significance. We illustrate the statistical features including type-I-error control and power of the proposed method through extensive numerical studies. Applying our method to the UK Biobank dataset, we showcase the practical utility of the proposed method, revealing SNPs and genes with strong potential for latent interaction effects.
期刊介绍:
PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill).
Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.