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A Bayesian Framework to Account for Complex Non-Genetic Factors in Gene Expression Levels Greatly Increases Power in eQTL Studies

机译:用于在基因表达水平上解释复杂的非遗传因素的贝叶斯框架极大地提高了eQTL研究的能力

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摘要

Gene expression measurements are influenced by a wide range of factors, such as the state of the cell, experimental conditions and variants in the sequence of regulatory regions. To understand the effect of a variable of interest, such as the genotype of a locus, it is important to account for variation that is due to confounding causes. Here, we present VBQTL, a probabilistic approach for mapping expression quantitative trait loci (eQTLs) that jointly models contributions from genotype as well as known and hidden confounding factors. VBQTL is implemented within an efficient and flexible inference framework, making it fast and tractable on large-scale problems. We compare the performance of VBQTL with alternative methods for dealing with confounding variability on eQTL mapping datasets from simulations, yeast, mouse, and human. Employing Bayesian complexity control and joint modelling is shown to result in more precise estimates of the contribution of different confounding factors resulting in additional associations to measured transcript levels compared to alternative approaches. We present a threefold larger collection of cis eQTLs than previously found in a whole-genome eQTL scan of an outbred human population. Altogether, 27% of the tested probes show a significant genetic association in cis, and we validate that the additional eQTLs are likely to be real by replicating them in different sets of individuals. Our method is the next step in the analysis of high-dimensional phenotype data, and its application has revealed insights into genetic regulation of gene expression by demonstrating more abundant cis-acting eQTLs in human than previously shown. Our software is freely available online at .
机译:基因表达测量受多种因素影响,例如细胞状态,实验条件和调控区序列的变异。要了解目标变量(例如基因座的基因型)的作用,重要的是要考虑由于混杂原因引起的变异。在这里,我们介绍了VBQTL,这是一种映射表达定量性状基因座(eQTL)的概率方法,该方法共同对基因型以及已知和隐藏的混杂因素的贡献进行建模。 VBQTL是在高效且灵活的推理框架中实现的,因此可以快速且易于处理大规模问题。我们将VBQTL的性能与处理模拟,酵母,小鼠和人类的eQTL映射数据集上的混杂变异性的替代方法进行比较。结果表明,与其他方法相比,采用贝叶斯复杂度控制和联合建模可以更精确地估计不同混杂因素的贡献,从而导致与测得的笔录水平产生更多关联。我们提出的顺式eQTL的集合比以前在异族人群的全基因组eQTL扫描中发现的三倍大。总共,有27%的受测探针在顺式中显示出显着的遗传关联,我们通过在不同的个体中复制它们来验证额外的eQTL可能是真实的。我们的方法是分析高维表型数据的下一步,它的应用通过证明人体内比以前显示的丰富的顺式作用eQTL,揭示了对基因表达遗传调控的见识。我们的软件可在上免费在线获取。

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