4.7 Review

Computational Methods for Mapping, Assembly and Quantification for Coding and Non-coding Transcripts

期刊

出版社

ELSEVIER
DOI: 10.1016/j.csbj.2019.04.012

关键词

RNA-Seq; Transctipt; Genome; Transposable element; Long non-coding RNA

资金

  1. National Natural Science Foundation of China [31850410463, 31850410486]
  2. Shenzhen Peacock plan
  3. Shenzhen Science and Technology Innovation Committee general program [JCYJ20170307110638890]

向作者/读者索取更多资源

The measurement of gene expression has long provided significant insight into biological functions. The development of high-throughput short-read sequencing technology has revealed transcriptional complexity at an unprecedented scale, and informed almost all areas of biology. However, as researchers have sought to gather more insights from the data, these new technologies have also increased the computational analysis burden. In this review, we describe typical computational pipelines for RNA-Seq analysis and discuss their strengths and weaknesses for the assembly, quantification and analysis of coding and non-coding RNAs. We also discuss the assembly of transposable elements into transcripts, and the difficulty these repetitive elements pose. In summary, RNA-Seq is a powerful technology that is likely to remain a key asset in the biologist's toolkit. (C) 2019 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据