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MCPerm: A Monte Carlo Permutation Method for Accurately Correcting the Multiple Testing in a Meta-Analysis of Genetic Association Studies

机译:MCPerm:蒙特卡洛置换方法,用于准确校正遗传关联研究的荟萃分析中的多重检验

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摘要

Traditional permutation (TradPerm) tests are usually considered the gold standard for multiple testing corrections. However, they can be difficult to complete for the meta-analyses of genetic association studies based on multiple single nucleotide polymorphism loci as they depend on individual-level genotype and phenotype data to perform random shuffles, which are not easy to obtain. Most meta-analyses have therefore been performed using summary statistics from previously published studies. To carry out a permutation using only genotype counts without changing the size of the TradPerm P-value, we developed a Monte Carlo permutation (MCPerm) method. First, for each study included in the meta-analysis, we used a two-step hypergeometric distribution to generate a random number of genotypes in cases and controls. We then carried out a meta-analysis using these random genotype data. Finally, we obtained the corrected permutation P-value of the meta-analysis by repeating the entire process N times. We used five real datasets and five simulation datasets to evaluate the MCPerm method and our results showed the following: (1) MCPerm requires only the summary statistics of the genotype, without the need for individual-level data; (2) Genotype counts generated by our two-step hypergeometric distributions had the same distributions as genotype counts generated by shuffling; (3) MCPerm had almost exactly the same permutation P-values as TradPerm (r = 0.999; P<2.2e-16); (4) The calculation speed of MCPerm is much faster than that of TradPerm. In summary, MCPerm appears to be a viable alternative to TradPerm, and we have developed it as a freely available R package at CRAN: .
机译:传统的置换(TradPerm)测试通常被认为是多次测试校正的黄金标准。然而,由于它们依赖于个体水平的基因型和表型数据来进行随机改组,因此难以完成基于多个单核苷酸多态性基因座的遗传关联研究的荟萃分析。因此,大多数荟萃分析都是使用以前发表的研究的摘要统计数据进行的。为了仅使用基因型计数进行排列而不改变TradPerm P值的大小,我们开发了蒙特卡洛排列(MCPerm)方法。首先,对于纳入荟萃分析的每项研究,我们采用两步超几何分布在病例和对照中产生随机数的基因型。然后,我们使用这些随机基因型数据进行了荟萃分析。最后,通过重复整个过程N次,获得了荟萃分析的校正置换P值。我们使用五个真实的数据集和五个模拟数据集来评估MCPerm方法,结果表明:(1)MCPerm仅需要基因型的摘要统计,而无需个体水平的数据; (2)两步超几何分布产生的基因型计数与改组产生的基因型计数具有相同的分布; (3)MCPerm的排列P值与TradPerm几乎完全相同(r = 0.999; P <2.2e-16); (4)MCPerm的计算速度比TradPerm快得多。总而言之,MCPerm似乎是TradPerm的可行替代品,我们已经将其开发为CRAN:上免费提供的R包。

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