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Using Principal Components of Genetic Variation for Robust and Powerful Detection of Gene-Gene Interactions in Case-Control and Case-Only Studies

机译:利用遗传变异的主要成分对病例-对照和仅病例研究中的基因-基因相互作用进行稳健而有力的检测

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摘要

Many popular methods for exploring gene-gene interactions, including the case-only approach, rely on the key assumption that physically distant loci are in linkage equilibrium in the underlying population. These methods utilize the presence of correlation between unlinked loci in a disease-enriched sample as evidence of interactions among the loci in the etiology of the disease. We use data from the CGEMS case-control genome-wide association study of breast cancer to demonstrate empirically that the case-only and related methods have the potential to create large-scale false positives because of the presence of population stratification (PS) that creates long-range linkage disequilibrium in the genome. We show that the bias can be removed by considering parametric and nonparametric methods that assume gene-gene independence between unlinked loci, not in the entire population, but only conditional on population substructure that can be uncovered based on the principal components of a suitably large panel of PS markers. Applications in the CGEMS study as well as simulated data show that the proposed methods are robust to the presence of population stratification and are yet much more powerful, relative to standard logistic regression methods that are also commonly used as robust alternatives to the case-only type methods.
机译:许多流行的探索基因与基因相互作用的方法,包括仅基于案例的方法,都基于以下关键假设:物理距离较远的基因座在基础种群中处于连锁平衡状态。这些方法利用了疾病富集样本中未连接基因座之间相关性的存在,作为疾病病因学中基因座之间相互作用的证据。我们使用来自CGEMS病例对照全基因组乳腺癌研究的数据来通过经验证明,仅病例和相关方法有可能产生大规模假阳性,因为存在人口分层(PS)基因组中的远程连锁不平衡。我们表明可以通过考虑参数化和非参数化方法来消除偏见,这些方法假定未关联基因座之间的基因-基因独立性,而不是在整个人群中,而仅取决于可以基于适当大面板的主要组成部分才能揭示的人群亚结构PS标记。在CGEMS研究中的应用以及模拟数据表明,相对于通常也仅作为案例类型的可靠替代方法的标准逻辑回归方法,所提出的方法对存在人口分层具有鲁棒性,但功能强大得多。方法。

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