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Analyze multivariate phenotypes in genetic association studies by combining univariate association tests.

机译:通过结合单变量关联测试来分析遗传关联研究中的多元表型。

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Multivariate phenotypes are frequently encountered in genome-wide association studies (GWAS). Such phenotypes contain more information than univariate phenotypes, but how to best exploit the information to increase the chance of detecting genetic variant of pleiotropic effect is not always clear. Moreover, when multivariate phenotypes contain a mixture of quantitative and qualitative measures, limited methods are applicable. In this paper, we first evaluated the approach originally proposed by O'Brien and by Wei and Johnson that combines the univariate test statistics and then we proposed two extensions to that approach. The original and proposed approaches are applicable to a multivariate phenotype containing any type of components including continuous, categorical and survival phenotypes, and applicable to samples consisting of families or unrelated samples. Simulation results suggested that all methods had valid type I error rates. Our extensions had a better power than O'Brien's method with heterogeneous means among univariate test statistics, but were less powerful than O'Brien's with homogeneous means among individual test statistics. All approaches have shown considerable increase in power compared to testing each component of a multivariate phenotype individually in some cases. We apply all the methods to GWAS of serum uric acid levels and gout with 550,000 single nucleotide polymorphisms in the Framingham Heart Study.
机译:在全基因组关联研究(GWAS)中经常遇到多元表型。这种表型比单变量表型包含更多的信息,但是如何最好地利用这些信息来增加检测多效性效应遗传变异的机会并不总是很清楚。此外,当多元表型包含定量和定性指标的混合物时,适用的方法有限。在本文中,我们首先评估了O'Brien和Wei and Johnson最初提出的结合单变量检验统计量的方法,然后提出了对该方法的两个扩展。原始和建议的方法适用于包含任何类型成分的多元表型,包括连续,分类和生存表型,并且适用于由家族或无关样品组成的样品。仿真结果表明,所有方法均具有有效的I类错误率。在单变量测试统计数据中,我们的扩展具有比使用异类均值的O'Brien方法更好的功效,但在单个测试统计数据中,其扩展效果不如具有均等均值的O'Brien方法。与在某些情况下分别测试多元表型的每个组成部分相比,所有方法都显示出了强大的功能。在弗雷明汉心脏研究中,我们将所有方法应用于血清尿酸水平和痛风的GWAS,并具有5​​50,000个单核苷酸多态性。

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