单变量
多效性
全基因组关联研究
遗传建筑学
多元统计
生物
单核苷酸多态性
结构方程建模
遗传关联
遗传学
进化生物学
计算生物学
数量性状位点
表型
统计
数学
基因
基因型
作者
Andrew D. Grotzinger,Mijke Rhemtulla,Ronald de Vlaming,Stuart J. Ritchie,Travis T. Mallard,W. David Hill,Hill F. Ip,Riccardo E. Marioni,Andrew M. McIntosh,Ian J. Deary,Philipp Koellinger,K. Paige Harden,Michel G. Nivard,Elliot M. Tucker‐Drob
标识
DOI:10.1038/s41562-019-0566-x
摘要
Genetic correlations estimated from genome-wide association studies (GWASs) reveal pervasive pleiotropy across a wide variety of phenotypes. We introduce genomic structural equation modelling (genomic SEM): a multivariate method for analysing the joint genetic architecture of complex traits. Genomic SEM synthesizes genetic correlations and single-nucleotide polymorphism heritabilities inferred from GWAS summary statistics of individual traits from samples with varying and unknown degrees of overlap. Genomic SEM can be used to model multivariate genetic associations among phenotypes, identify variants with effects on general dimensions of cross-trait liability, calculate more predictive polygenic scores and identify loci that cause divergence between traits. We demonstrate several applications of genomic SEM, including a joint analysis of summary statistics from five psychiatric traits. We identify 27 independent single-nucleotide polymorphisms not previously identified in the contributing univariate GWASs. Polygenic scores from genomic SEM consistently outperform those from univariate GWASs. Genomic SEM is flexible and open ended, and allows for continuous innovation in multivariate genetic analysis.
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