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Elucidating the editome: bioinformatics approaches for RNA editing detection

机译:阐明编辑组:Bioinfinomatics用于RNA编辑检测方法

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摘要

RNA editing is a widespread co/posttranscriptional mechanism affecting primary RNAs by specific nucleotide modifications, which plays relevant roles in molecular processes including regulation of gene expression and/or the processing of noncoding RNAs. In recent years, the detection of editing sites has been improved through the availability of high-throughput RNA sequencing (RNA-Seq) technologies. Accurate bioinformatics pipelines are essential for the analysis of next-generation sequencing (NGS) data to ensure the correct identification of edited sites. Several pipelines, using various read mappers and variant callers with a wide range of adjustable parameters, are available for the detection of RNA editing events. In this review, we discuss some of the most recent and popular tools and provide guidelines for RNA-Seq data generation and analysis for the detection of RNA editing in massive transcriptome data. Using simulated and real data sets, we provide an overview of their behavior, emphasizing the fact that the RNA editing detection in NGS data sets remains a challenging task.
机译:RNA编辑是通过特定核苷酸修饰影响初级RNA的广泛CO /后术语机制,其在分子过程中起着相关的作用,包括调节基因表达和/或非编码RNA的加工。近年来,通过高通量RNA测序(RNA-SEQ)技术的可用性改善了编辑部位的检测。准确的生物信息学管道对于分析下一代测序(NGS)数据至关重要,以确保正确识别编辑的网站。使用各种读取映射器和具有各种可调参数的各种读取映射器和变体呼叫者的若干管道可用于检测RNA编辑事件。在这篇综述中,我们讨论了一些最新和流行的工具,并为RNA-SEQ数据生成和分析提供了巨大转录组数据中RNA编辑的分析。使用模拟和实际数据集,我们提供了他们的行为概述,强调NGS数据集中的RNA编辑检测仍然是一个具有挑战性的任务。

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