Bioconductor version: Release (2.12)
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 newcastle.edu.au>
To install this package, start R and enter:
source("http://bioconductor.org/biocLite.R") biocLite("SeqGSEA")
To cite this package in a publication, start R and enter:
citation("SeqGSEA")
R Script | Gene set enrichment analysis of RNA-Seq data with the SeqGSEA package | |
Reference Manual |
biocViews | DifferentialExpression, GeneExpression, GeneSetEnrichment, HighThroughputSequencing, RNAseq, Software |
Version | 1.0.2 |
In Bioconductor since | BioC 2.13 (R-2.18) |
License | GPL (>= 3) |
Depends | Biobase, DESeq, biomaRt, foreach |
Imports | methods, doParallel |
Suggests | |
System Requirements | |
URL | |
Depends On Me | |
Imports Me | |
Suggests Me |
Package Source | SeqGSEA_1.0.2.tar.gz |
Windows Binary | SeqGSEA_1.0.2.zip (32- & 64-bit) |
Mac OS X 10.6 (Snow Leopard) | SeqGSEA_1.0.2.tgz |
Package Downloads Report | Download Stats |
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