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Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies

机译:基因和途径水平方法作为全基因组关联研究的二级分析的相对性能

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摘要

BackgroundDespite the success of genome-wide association studies (GWAS), there still remains “missing heritability” for many traits. One contributing factor may be the result of examining one marker at a time as opposed to a group of markers that are biologically meaningful in aggregate. To address this problem, a variety of gene- and pathway-level methods have been developed to identify putative biologically relevant associations. A simulation was conducted to systematically assess the performance of these methods. Using genetic data from 4,500 individuals in the Wellcome Trust Case Control Consortium (WTCCC), case–control status was simulated based on an additive polygenic model. We evaluated gene-level methods based on their sensitivity, specificity, and proportion of false positives. Pathway-level methods were evaluated on the relationship between proportion of causal genes within the pathway and the strength of association.
机译:背景尽管全基因组关联研究(GWAS)取得了成功,但许多性状仍然“缺乏遗传性”。一个促成因素可能是一次检查一个标志物的结果,而不是一组生物学上有意义的标志物的结果。为了解决这个问题,已经开发了多种基因和途径水平的方法来鉴定推测的生物学相关的关联。进行了仿真以系统地评估这些方法的性能。利用来自威康信托案例控制协会(WTCCC)的4,500个人的遗传数据,基于加性多基因模型对案例控制状态进行了模拟。我们根据其敏感性,特异性和假阳性比例评估了基因水平的方法。评估了通路水平方法对通路内因果基因比例与关联强度之间的关系。

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