A Bayesian model to identify multiple expression patterns with simultaneous FDR control for a multi-factor RNA-seq experiment.

IF 0.9 4区 数学 Q3 Mathematics
Yuanyuan Bian, Chong He, Jing Qiu
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引用次数: 0

Abstract

It is often of research interest to identify genes that satisfy a particular expression pattern across different conditions such as tissues, genotypes, etc. One common practice is to perform differential expression analysis for each condition separately and then take the intersection of differentially expressed (DE) genes or non-DE genes under each condition to obtain genes that satisfy a particular pattern. Such a method can lead to many false positives, especially when the desired gene expression pattern involves equivalent expression under one condition. In this paper, we apply a Bayesian partition model to identify genes of all desired patterns while simultaneously controlling their false discovery rates (FDRs). Our simulation studies show that the common practice fails to control group specific FDRs for patterns involving equivalent expression while the proposed Bayesian method simultaneously controls group specific FDRs at all settings studied. In addition, the proposed method is more powerful when the FDR of the common practice is under control for identifying patterns only involving DE genes. Our simulation studies also show that it is an inherently more challenging problem to identify patterns involving equivalent expression than patterns only involving differential expression. Therefore, larger sample sizes are required to obtain the same target power to identify the former types of patterns than the latter types of patterns.

一个贝叶斯模型,以识别多种表达模式与同时FDR控制的多因素RNA-seq实验。
识别在不同条件下(如组织、基因型等)满足特定表达模式的基因通常是研究兴趣。一种常见的做法是分别对每种情况进行差异表达分析,然后取每种情况下差异表达(DE)基因或非DE基因的交集,获得满足特定模式的基因。这种方法可能导致许多假阳性,特别是当所需的基因表达模式在一种条件下涉及等效表达时。在本文中,我们应用贝叶斯分割模型来识别所有期望模式的基因,同时控制它们的错误发现率(FDRs)。我们的模拟研究表明,对于涉及等效表达的模式,通常的做法无法控制组特定fdr,而所提出的贝叶斯方法同时控制了在所研究的所有设置下的组特定fdr。此外,当通用实践的FDR在识别仅涉及DE基因的模式的控制下时,所提出的方法更强大。我们的模拟研究还表明,识别涉及等效表达的模式比仅涉及差分表达的模式本质上更具挑战性。因此,与识别后一种模式相比,需要更大的样本量来获得识别前一种模式类型的相同目标功率。
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来源期刊
CiteScore
1.20
自引率
11.10%
发文量
8
审稿时长
6-12 weeks
期刊介绍: Statistical Applications in Genetics and Molecular Biology seeks to publish significant research on the application of statistical ideas to problems arising from computational biology. The focus of the papers should be on the relevant statistical issues but should contain a succinct description of the relevant biological problem being considered. The range of topics is wide and will include topics such as linkage mapping, association studies, gene finding and sequence alignment, protein structure prediction, design and analysis of microarray data, molecular evolution and phylogenetic trees, DNA topology, and data base search strategies. Both original research and review articles will be warmly received.
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