RNA-Seq Data: A Complexity Journey

被引:9
|
作者
Capobianco, Enrico [1 ,2 ]
机构
[1] Univ Miami, Ctr Computat Sci, Miami, FL 33124 USA
[2] IFC CNR, Lab Integrat Syst Med, Pisa, Italy
来源
关键词
Transcriptome profiling; RNA-Seq; Complexity; Inverse problems; Networks;
D O I
10.1016/j.csbj.2014.09.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A paragraph from the highlights of "Transcriptomics: Throwing light on dark matter" by L. Flintoft (Nature Reviews Genetics 11, 455, 2010), says: "Reports over the past few years of extensive transcription throughout eukaryotic genomes have led to considerable excitement. However, doubts have been raised about the methods that have detected this pervasive transcription and about how much of it is functional." Since the appearance of the ENCODE project and due to follow-up work, a shift from the pervasive transcription observed from RNA-Seq data to its functional validation is gradually occurring. However, much less attention has been turned to the problem of deciphering the complexity of transcriptome data, which determines uncertainty with regard to identification, quantification and differential expression of genes and non-coding RNAs. The aim of this mini-review is to emphasize transcriptome-related problems of direct and inverse nature for which novel inference approaches are needed. (C) 2014 Capobianco. Published by Elsevier B.V. on behalf of the Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:123 / 130
页数:8
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