| Literature DB >> 31768069 |
Longda Jiang1, Zhili Zheng1,2, Ting Qi1, Kathryn E Kemper1, Naomi R Wray1,3, Peter M Visscher1, Jian Yang4,5.
Abstract
The genome-wide association study (GWAS) has been widely used as an experimental design to detect associations between genetic variants and a phenotype. Two major confounding factors, population stratification and relatedness, could potentially lead to inflated GWAS test statistics and hence to spurious associations. Mixed linear model (MLM)-based approaches can be used to account for sample structure. However, genome-wide association (GWA) analyses in biobank samples such as the UK Biobank (UKB) often exceed the capability of most existing MLM-based tools especially if the number of traits is large. Here, we develop an MLM-based tool (fastGWA) that controls for population stratification by principal components and for relatedness by a sparse genetic relationship matrix for GWA analyses of biobank-scale data. We demonstrate by extensive simulations that fastGWA is reliable, robust and highly resource-efficient. We then apply fastGWA to 2,173 traits on array-genotyped and imputed samples from 456,422 individuals and to 2,048 traits on whole-exome-sequenced samples from 46,191 individuals in the UKB.Mesh:
Year: 2019 PMID: 31768069 DOI: 10.1038/s41588-019-0530-8
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330