目录

SeqGSEA

The package generally provides methods for gene set enrichment analysis of high-throughput RNA-Seq data by integrating differential expression and splicing. It uses negative binomial distribution to model read count data, which accounts for sequencing biases and biological variation. Based on permutation tests, statistical significance can also be achieved regarding each gene’s differential expression and splicing, respectively.

  • Author: Xi Wang (Xi.Wang at newcastle.edu.au)

  • Maintainer: Xi Wang (Xi.Wang at dkfz-heidelberg.de)

Citation

Wang X and Cairns MJ (2013). “Gene Set Enrichment Analysis of RNA-Seq Data: Integrating Differential Expression and Splicing.” BMC Bioinformatics, 14(Suppl 5), pp. S16.

Wang X and Cairns MJ (2014). “SeqGSEA: a Bioconductor package for gene set enrichment analysis of RNA-Seq data integrating differential expression and splicing.” Bioinformatics, 30(12), pp. 1777-9.

  • from within R, enter citation("SeqGSEA")

Installation

To install this package, start R and enter:

  source("https://bioconductor.org/biocLite.R")
  biocLite("SeqGSEA")

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

  browseVignettes("SeqGSEA")
关于

用于基因集富集分析的R包,整合RNA-seq表达差异和剪接差异数据

980.0 KB
邀请码
    Gitlink(确实开源)
  • 加入我们
  • 官网邮箱:gitlink@ccf.org.cn
  • QQ群
  • QQ群
  • 公众号
  • 公众号

版权所有:中国计算机学会技术支持:开源发展技术委员会
京ICP备13000930号-9 京公网安备 11010802047560号