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Kernel machine SNP-set testing under multiple candidate kernels

机译:多个候选内核下的内核机器SNP集测试

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摘要

Joint testing for the cumulative effect of multiple single-nucleotide polymorphisms grouped on the basis of prior biological knowledge has become a popular and powerful strategy for the analysis of large-scale genetic association studies. The kernel machine (KM)-testing framework is a useful approach that has been proposed for testing associations between multiple genetic variants and many different types of complex traits by comparing pairwise similarity in phenotype between subjects to pairwise similarity in genotype, with similarity in genotype defined via a kernel function. An advantage of the KM framework is its flexibility: choosing different kernel functions allows for different assumptions concerning the underlying model and can allow for improved power. In practice, it is difficult to know which kernel to use a priori because this depends on the unknown underlying trait architecture and selecting the kernel which gives the lowest P-value can lead to inflated type I error. Therefore, we propose practical strategies for KM testing when multiple candidate kernels are present based on constructing composite kernels and based on efficient perturbation procedures. We demonstrate through simulations and real data applications that the procedures protect the type I error rate and can lead to substantially improved power over poor choices of kernels and only modest differences in power vs. using the best candidate kernel.
机译:在先验生物学知识的基础上对多个单核苷酸多态性的累积效应进行联合测试已成为分析大规模遗传关联研究的一种流行而有力的策略。内核机器(KM)测试框架是一种有用的方法,已提出用于通过比较受试者之间的表型成对相似性与基因型的成对相似性(定义了基因型的相似性)来测试多个遗传变异与许多不同类型的复杂性状之间的关联的方法通过内核函数。 KM框架的一个优点是它的灵活性:选择不同的内核功能可以对基础模型进行不同的假设,并可以提高性能。在实践中,很难知道要使用哪个先验内核,因为这取决于未知的基础特征体系结构,选择具有最低P值的内核可能会导致I型错误膨胀。因此,基于构造复合内核并基于有效的扰动过程,当存在多个候选内核时,我们提出了用于KM测试的实用策略。通过仿真和实际数据应用,我们证明了该程序可以保护I型错误率,并且可以在选择不良的内核时显着提高功耗,并且与使用最佳候选内核相比,功耗只有适度的差异。

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