RNA-Seq是现代转录组学研究的有效工具

M. Mekso, T. Feyissa
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引用次数: 1

摘要

转录组分析是鉴定和了解基因的有效方法。寻找不同条件下表达差异的基因是转录组学的一个关键方面。RNA序列的发现使下一代测序技术发生了革命性的变化。事实上,RNA测序不需要基因探针,并在更大范围内提供基因表达的精确测量,这证明了它比其他常用技术更可靠。表达的基因谱和转录组数据存储在数据库中,可以自由访问。在RNA序列短读映射到参考转录组(一个物种的所有已知转录RNA序列的集合)或数据库中的基因组时,各种数据库搜索工具和比对方法变得可见。有各种各样的应用程序可以帮助对齐由片段测序产生的短读取。表达基因的研究是通过量化与参考基因组或转录组相一致的读数来辅助的。除了差异基因表达外,RNA测序还提供了关于备选剪接和基因同种异构体的重要信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA-Seq as an Effective Tool for Modern Transcriptomics, A Review-based Study
Transcriptome analysis is a useful method for identification and understanding genes. Finding genes that are differentially expressed between conditions is a crucial aspect of transcriptomics. The discovery of RNA seq has been revolutionized next-generation sequencing technology. The fact that RNA sequencing does not requires gene probes and provides a precise measure of gene expression over a much wider range proved its credibility over other common techniques. The expressed gene profile and transcriptome data are stored in a database and could be accessed freely. During RNA seq short read mapping to the reference transcriptome (the set of all known transcript RNA sequences for a species) or genome in the database, a variety of database search tools and alignment methods become visible. There are a variety of applications that help align short reads generated by fragment sequencing. The study of expressed genes is aided by quantifying reads that align to the reference genome or transcriptome. RNA sequencing gives crucial information regarding alternative splicing and gene isoforms, in addition to differential gene expression.
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