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A length bias corrected likelihood ratio test for the detection of differentially expressed pathways in RNA-Seq data

机译:用于检测RNA-SEQ数据中差异表达途径的长度偏置校正似然比测试

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RNA-Seq has become an important alternative to microarrays in transcriptomic studies. The unique features of count-based RNA-Seq data pose new challenges for pathway analysis and call for new computational tools. In this study, we developed a likelihood ratio test to identify differentially expressed pathways in RNA-Seq data. The proposed method takes into account the coherent gene expression patterns by considering a common variance component shared by genes within a pathway. Additionally, we implemented a method to correct the length bias existing in the differential expression analysis using RNA-Seq data, where longer transcripts are more likely to be identified as differentially expressed. We demonstrated the ability of the proposed method using both synthetic and real data. We found that the top differentially expressed pathways between liver and kidney tissue samples identified using our method are associated with organ-specific functions.
机译:RNA-SEQ已成为转录组研究中微阵列的重要替代方案。基于计数的RNA-SEQ数据的独特特征对途径分析的新挑战并呼叫新的计算工具。在这项研究中,我们开发了一种似然比测试,以识别RNA-SEQ数据中的差异表达途径。所提出的方法通过考虑在途径内基因共享的常见方差组分来考虑相干基因表达模式。另外,我们实现了一种方法来校正使用RNA-SEQ数据在差异表达分析中存在的长度偏差,其中更容易被识别为差异表达的更长的转录物。我们展示了所提出的方法使用合成和实际数据的能力。我们发现,使用我们的方法鉴定的肝脏和肾脏组织样本之间的顶部差异表达途径与器官特定功能有关。

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