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Integrative set enrichment testing for multiple omics platforms

机译:多个OMICS平台的集成型富集测试

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Background Enrichment testing assesses the overall evidence of differential expression behavior of the elements within a defined set. When we have measured many molecular aspects, e.g. gene expression, metabolites, proteins, it is desirable to assess their differential tendencies jointly across platforms using an integrated set enrichment test. In this work we explore the properties of several methods for performing a combined enrichment test using gene expression and metabolomics as the motivating platforms. Results Using two simulation models we explored the properties of several enrichment methods including two novel methods: the logistic regression 2-degree of freedom Wald test and the 2-dimensional permutation p-value for the sum-of-squared statistics test. In relation to their univariate counterparts we find that the joint tests can improve our ability to detect results that are marginal univariately. We also find that joint tests improve the ranking of associated pathways compared to their univariate counterparts. However, there is a risk of Type I error inflation with some methods and self-contained methods lose specificity when the sets are not representative of underlying association. Conclusions In this work we show that consideration of data from multiple platforms, in conjunction with summarization via a priori pathway information, leads to increased power in detection of genomic associations with phenotypes.
机译:背景技术浓缩测试评估确定集中元素的差异表达行为的总体证据。当我们测量许多分子方面时,例如基因表达,代谢物,蛋白质,期望使用集成型富集试验在平台上共同评估它们的差异趋势。在这项工作中,我们探讨了使用基因表达和代谢组织作为激励平台进行组合富集试验的几种方法的性质。结果采用两种仿真模型,我们探讨了多种浓缩方法的性质,包括两种新方法:Logistic回归2-自由度沃尔德测试和平方和平方和平方级别测试的二维置换P值。与他们的单变量同行有关,我们发现联合试验可以改善我们检测到边际不变的结果的能力。我们还发现,与单束同行相比,联合试验改善了相关途径的排名。然而,当集合不代表底层关联时,存在有一些方法的I型误差通胀的风险,并且自包含的方法失去特异性。结论在这项工作中,我们表明,通过先验路径信息的概述,与多个平台的数据考虑到多个平台的数据,导致在与表型检测基因组关联的力量增加。

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