Bioinformatics for RNA‐Seq Data Analysis ( Bioinformatics - Updated Features and Applications )

Publication series : Bioinformatics - Updated Features and Applications

Author: Shanrong Zhao Baohong Zhang Ying Zhang William Gordon5  

Publisher: IntechOpen‎

Publication year: 2016

E-ISBN: INT6142163267

P-ISBN(Paperback): 9789535125464

P-ISBN(Hardback):  9789535125471

Subject: Q5 Biochemistry

Keyword: 生物化学

Language: ENG

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Bioinformatics for RNA‐Seq Data Analysis

Description

While RNA sequencing (RNA‐seq) has become increasingly popular for transcriptome profiling, the analysis of the massive amount of data generated by large‐scale RNA‐seq still remains a challenge. RNA‐seq data analyses typically consist of (1) accurate mapping of millions of short sequencing reads to a reference genome, including the identification of splicing events; (2) quantifying expression levels of genes, transcripts, and exons; (3) differential analysis of gene expression among different biological conditions; and (4) biological interpretation of differentially expressed genes. Despite the fact that multiple algorithms pertinent to basic analyses have been developed, there are still a variety of unresolved questions. In this chapter, we review the main tools and algorithms currently available for RNA‐seq data analyses, and our goal is to help RNA‐seq data analysts to make an informed choice of tools in practical RNA‐seq data analysis. In the meantime, RNA‐seq is evolving rapidly, and newer sequencing technologies are briefly introduced, including stranded RNA‐seq, targeted RNA‐seq, and single‐cell RNA‐seq.

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