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Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma

机译:使用eQTL权重提高全基因组关联研究的能力:儿童哮喘的遗传研究

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摘要

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.
机译:越来越多的证据表明,与复杂性状相关的单核苷酸多态性(SNP)更有可能是表达数量性状基因座(eQTL)。因此,整合eQTL信息有可能提高全基因组关联研究(GWAS)的能力。在本文中,我们建议在基于SNP的关联测试中使用eQTL权重作为先验信息,以提高测试能力,同时保持对家庭错误率(FWER)或错误发现率(FDR)的控制。我们将提出的方法应用于由1296名德国血统的无关个体组成的儿童哮喘的GWAS分析中。结果证实,eQTL富含先前报道的哮喘SNP。我们还发现,使用没有eQTL加权的过程,某些SNP并不重要,但是使用eQTL加权的Bonferroni或Benjamini-Hochberg过程,在控制相同的FWER或FDR水平的情况下,它们变得很重要。在最近的文献中,一些独立研究已经报道了其中一些SNP。结果表明,eQTL加权程序为提高GWAS的功能提供了一种有希望的方法。我们还报告了应用于大规模欧洲GABRIEL联盟数据的方法的结果。

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