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Comprehensive processing of high-throughput small RNA sequencing data including quality checking normalization and differential expression analysis using the UEA sRNA Workbench

机译:使用UEA sRNA Workbench全面处理高通量小RNA测序数据包括质量检查归一化和差异表达分析

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摘要

Recently, high-throughput sequencing (HTS) has revealed compelling details about the small RNA (sRNA) population in eukaryotes. These 20 to 25 nt noncoding RNAs can influence gene expression by acting as guides for the sequence-specific regulatory mechanism known as RNA silencing. The increase in sequencing depth and number of samples per project enables a better understanding of the role sRNAs play by facilitating the study of expression patterns. However, the intricacy of the biological hypotheses coupled with a lack of appropriate tools often leads to inadequate mining of the available data and thus, an incomplete description of the biological mechanisms involved. To enable a comprehensive study of differential expression in sRNA data sets, we present a new interactive pipeline that guides researchers through the various stages of data preprocessing and analysis. This includes various tools, some of which we specifically developed for sRNA analysis, for quality checking and normalization of sRNA samples as well as tools for the detection of differentially expressed sRNAs and identification of the resulting expression patterns. The pipeline is available within the UEA sRNA Workbench, a user-friendly software package for the processing of sRNA data sets. We demonstrate the use of the pipeline on a H. sapiens data set; additional examples on a B. terrestris data set and on an A. thaliana data set are described in the . A comparison with existing approaches is also included, which exemplifies some of the issues that need to be addressed for sRNA analysis and how the new pipeline may be used to do this.
机译:最近,高通量测序(HTS)揭示了有关真核生物中小RNA(sRNA)群体的令人信服的细节。这些20至25 nt的非编码RNA可以通过充当称为RNA沉默的序列特异性调控机制的指导来影响基因表达。每个项目的测序深度和样品数量的增加,通过促进表达模式的研究,使人们能够更好地了解sRNA的作用。但是,生物学假设的复杂性以及缺乏适当工具的情况常常导致对可用数据的挖掘不足,从而导致对所涉及生物学机制的描述不完整。为了全面研究sRNA数据集中的差异表达,我们提出了一条新的互动管道,指导研究人员完成数据预处理和分析的各个阶段。这包括各种工具,其中一些是我们专门开发用于sRNA分析的工具,用于sRNA样品的质量检查和归一化,以及用于检测差异表达的sRNA和鉴定所得表达模式的工具。该管道可在UEA sRNA Workbench中使用,UEA sRNA Workbench是用于处理sRNA数据集的用户友好软件包。我们演示了在智人数据集上使用管道的方法;陆地棉数据集和拟南芥数据集上的其他例子在。还包括与现有方法的比较,它举例说明了sRNA分析需要解决的一些问题,以及如何使用新管道来完成此任务。

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