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ABSSeq: a new RNA-Seq analysis method based on modelling absolute expression differences

机译:ABSSeq:一种基于绝对表达差异建模的新RNA-Seq分析方法

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Background The recent advances in next generation sequencing technology have made the sequencing of RNA (i.e., RNA-Seq) an extemely popular approach for gene expression analysis. Identification of significant differential expression represents a crucial initial step in these analyses, on which most subsequent inferences of biological functions are built. Yet, for identification of these subsequently analysed genes, most studies use an additional minimal threshold of differential expression that is not captured by the applied statistical procedures. Results Here we introduce a new analysis approach, ABSSeq, which uses a negative binomal distribution to model absolute expression differences between conditions, taking into account variations across genes and samples as well as magnitude of differences. In comparison to alternative methods, ABSSeq shows higher performance on controling type I error rate and at least a similar ability to correctly identify differentially expressed genes. Conclusions ABSSeq specifically considers the overall magnitude of expression differences, which enhances the power in detecting truly differentially expressed genes by reducing false positives at both very low and high expression level. In addition, ABSSeq offers to calculate shrinkage of fold change to facilitate gene ranking and effective outlier detection.
机译:背景技术下一代测序技术的最新进展已使RNA测序(即RNA-Seq)成为基因表达分析的一种非常流行的方法。在这些分析中,重要差异表达的鉴定代表了关键的第一步,在此基础上建立了生物学功能的大多数后续推论。然而,为了鉴定这些随后分析的基因,大多数研究使用了额外的最小差异表达阈值,该阈值未被应用的统计程序捕获。结果我们在这里介绍了一种新的分析方法ABSSeq,它使用负二项式分布来模拟条件之间的绝对表达差异,同时考虑到基因和样品之间的差异以及差异的大小。与替代方法相比,ABSSeq在控制I型错误率方面表现出更高的性能,并且至少具有正确识别差异表达基因的相似能力。结论ABSSeq特别考虑了表达差异的总体大小,通过降低极低和高表达水平的假阳性,增强了检测真正差异表达基因的能力。此外,ABSSeq还可以计算倍数变化的收缩,以促进基因排名和有效的离群值检测。

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