gsQTL: Associating genetic risk variants with gene sets by exploiting their shared variability

Gerard A Bouland, Niccolo Tesi, Ahmed Mahfouz, Marcel Reinders
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Abstract

To investigate the functional significance of genetic risk loci identified through genome-wide association studies (GWASs), genetic loci are linked to genes based on their capacity to account for variation in gene expression, resulting in expression quantitative trait loci (eQTL). Following this, gene set analyses are commonly used to gain insights into functionality. However, the efficacy of this approach is hampered by small effect sizes and the burden of multiple testing. We propose an alternative approach: instead of examining the cumulative associations of individual genes within a gene set, we consider the collective variation of the entire gene set. We introduce the concept of gene set QTL (gsQTL), and show it to be more adept at identifying links between genetic risk variants and specific gene sets. Notably, gsQTL experiences less susceptibility to inflation or deflation of significant enrichments compared with conventional methods. Furthermore, we demonstrate the broader applicability of shared variability within gene sets. This is evident in scenarios such as the coordinated regulation of genes by a transcription factor or coordinated differential expression.
gsQTL:利用基因组的共享变异性,将遗传风险变异与基因组联系起来
为了研究通过全基因组关联研究(GWAS)确定的遗传风险位点的功能意义,根据基因表达变异的能力将遗传位点与基因联系起来,形成表达定量性状位点(eQTL)。随后,基因组分析通常用于深入了解基因的功能。然而,这种方法的有效性受到效应大小小和多重测试负担的影响。我们提出了另一种方法:我们不研究基因集中单个基因的累积关联,而是考虑整个基因集的集体变异。我们引入了基因组 QTL(gsQTL)的概念,并证明它更善于识别遗传风险变异与特定基因组之间的联系。值得注意的是,与传统方法相比,gsQTL 不易受显著富集度膨胀或缩小的影响。此外,我们还证明了基因集内共享变异的广泛适用性。这在转录因子对基因的协调调控或协调差异表达等情况中都很明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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