Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma
Year: 2013
Type: article
Study design: Observational Study
Abstract: Increasing evidence suggests that single nucleotide polymorphisms (SNPs) associated with complex traits are more likely to be expression quantitative trait loci (eQTLs). Incorporating eQTL information hence has potential to increase power of genome-wide association studies (GWAS). In this paper, we propose using eQTL weights as prior information in SNP based association tests to improve test power while maintaining control of the family-wise error rate (FWER) or the false discovery rate (FDR). We apply the proposed methods to the analysis of a GWAS for childhood asthma consisting of 1296 unrelated individuals with German ancestry. The results confirm that eQTLs are enriched for previously reported asthma SNPs. We also find that some SNPs are insignificant using procedures without eQTL weighting, but become significant using eQTL-weighted Bonferroni or Benjamini-Hochberg procedures, while controlling the same FWER or FDR level. Some of these SNPs have been reported by independent studies in recent literature. The results suggest that the eQTL-weighted procedures provide a promising approach for improving power of GWAS. We also report the results of our methods applied to the large-scale European GABRIEL consortium data.
Source: Frontiers in Genetics
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $3,801
Awards: G1064917979, G1606511277, G2966453941, Genetics and Genomics and Respiratory Disease., Statistical Methods for Correlated and High-Dimensional Biomedical Data, Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics., Statistical Informatics for Cancer Research, Genetics and Genomics and Respiratory Disease., Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics., G8975541179
OpenAlex ID: W2145006442
