A survey of software for genome-wide discovery of differential splicing in RNA-Seq data

49Citations
Citations of this article
270Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Alternative splicing is a major contributor to cellular diversity. Therefore the identification and quantification of differentially spliced transcripts in genome-wide transcript analysis is an important consideration. Here, I review the software available for analysis of RNA-Seq data for differential splicing and discuss intrinsic challenges for differential splicing analyses. Three approaches to differential splicing analysis are described, along with their associated software implementations, their strengths, limitations, and caveats. Suggestions for future work include more extensive experimental validation to assess accuracy of the software predictions and consensus formats for outputs that would facilitate visualizations, data exchange, and downstream analyses. © 2014 Pitychoutis et al.; licensee BioMed Central Ltd.

Cite

CITATION STYLE

APA

Hooper, J. E. (2014). A survey of software for genome-wide discovery of differential splicing in RNA-Seq data. Human Genomics. Henry Stewart Publications. https://doi.org/10.1186/1479-7364-8-3

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free