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RNentropy: an entropy-based tool for the detection of significant variation of gene expression across multiple RNA-Seq experiments

机译:RNentropy:基于熵的工具用于检测多个RNA-Seq实验中基因表达的显着变化

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摘要

RNA sequencing (RNA-Seq) has become the experimental standard in transcriptome studies. While most of the bioinformatic pipelines for the analysis of RNA-Seq data and the identification of significant changes in transcript abundance are based on the comparison of two conditions, it is common practice to perform several experiments in parallel (e.g. from different individuals, developmental stages, tissues), for the identification of genes showing a significant variation of expression across all the conditions studied. In this work we present RNentropy, a methodology based on information theory devised for this task, which given expression estimates from any number of RNA-Seq samples and conditions identifies genes or transcripts with a significant variation of expression across all the conditions studied, together with the samples in which they are over- or under-expressed. To show the capabilities offered by our methodology, we applied it to different RNA-Seq datasets: 48 biological replicates of two different yeast conditions; samples extracted from six human tissues of three individuals; seven different mouse brain cell types; human liver samples from six individuals. Results, and their comparison to different state of the art bioinformatic methods, show that RNentropy can provide a quick and in depth analysis of significant changes in gene expression profiles over any number of conditions.
机译:RNA测序(RNA-Seq)已成为转录组研究的实验标准。尽管大多数用于分析RNA-Seq数据和确定转录本丰度显着变化的生物信息学流程都是基于两种条件的比较,但通常的做法是并行进行多个实验(例如,来自不同个体,发育阶段的实验) ,组织),以鉴定在所有研究条件下表现出明显表达差异的基因。在这项工作中,我们介绍了RNentropy,这是为此任务设计的基于信息论的方法,该方法可从任意数量的RNA-Seq样品中获得表达估计值,条件可识别在所有研究条件下表达均具有显着变化的基因或转录本,以及过表达或过表达的样本。为了展示我们的方法所提供的功能,我们将其应用于不同的RNA-Seq数据集:两种不同酵母条件的48个生物学重复;从三个人的六个人体组织中提取的样品;七种不同的小鼠脑细胞类型;六个人的人肝样本。结果及其与不同技术水平的生物信息学方法的比较结果表明,RNentropy可对各种条件下基因表达谱的重大变化提供快速而深入的分析。

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