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An adaptive gene-based test for methylation data

机译:基于适应性基因的甲基化数据测试

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DNA methylation plays an important role in normal human development and disease. In epigenome-wide association studies (EWAS), a univariate test for association between a phenotype and each cytosine-phosphate-guanine (CpG) site has been widely used. Given the number of CpG sites tested in EWAS, a stringent significance cutoff is required to adjust for multiple testing; in addition, multiple nearby CpG sites may be associated with the phenotype, which is ignored by a univariate test. These two factors may contribute to the power loss of a univariate test. As an alternative, we propose applying an adaptive gene-based test that is powerful in genome-wide association studies (GWAS), called aSPUw , to EWAS for simultaneous testing on multiple CpG sites within or near a gene. We show its application to the GAW20 methylation data set.
机译:DNA甲基化在正常人类发育和疾病中起着重要作用。在表观基因组范围的关联研究(EWAS)中,表型与每个胞嘧啶-磷酸-鸟嘌呤(CpG)位点之间的关联的单变量测试已被广泛使用。鉴于在EWAS中测试的CpG站点数量,需要严格的显着性临界值才能进行多次测试调整。此外,附近的多个CpG位点可能与该表型相关联,单变量检验忽略了该表型。这两个因素可能会导致单变量测试的功率损耗。作为替代方案,我们建议将在a全基因组关联研究(GWAS)中称为aSPUw的功能强大的基于自适应基因的测试应用于EWAS,以同时测试基因内或附近的多个CpG位点。我们将其应用于GAW20甲基化数据集。

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