easyRNASeq

Count summarization and normalization for RNA-Seq data.

Bioconductor version: Development (2.13)

Calculates the coverage of high-throughput short-reads against a genome of reference and summarizes it per feature of interest (e.g. exon, gene, transcript). The data can be normalized as 'RPKM' or by the 'DESeq' or 'edgeR' package.

Author: Nicolas Delhomme, Ismael Padioleau

Maintainer: Nicolas Delhomme <delhomme at embl.de>

To install this package, start R and enter:

    source("http://bioconductor.org/biocLite.R")
    biocLite("easyRNASeq")

To cite this package in a publication, start R and enter:

    citation("easyRNASeq")

Documentation

PDF R Script RNA-Seq
PDF   Reference Manual
Text   NEWS

Details

biocViews GeneExpression, Genetics, Preprocessing, RNAseq, Software
Version 1.7.1
In Bioconductor since BioC 2.10 (R-2.15)
License Artistic-2.0
Depends graphics, methods, parallel, utils, genomeIntervals(>= 1.15.0), Biobase(>= 2.19.0), BiocGenerics(>= 0.5.0), biomaRt(>= 2.15.0), edgeR(>= 3.1.0), Biostrings(>= 2.27.0), BSgenome(>= 1.27.0), DESeq(>= 1.11.0), GenomicRanges(>= 1.13.3), IRanges(>= 1.17.0), Rsamtools(>= 1.13.1), ShortRead(>= 1.17.0)
Imports
Suggests BSgenome.Dmelanogaster.UCSC.dm3(>= 1.3.17), GenomicFeatures(>= 1.11.0), RnaSeqTutorial(>= 0.0.11)
System Requirements
URL
Depends On Me RnaSeqTutorial
Imports Me
Suggests Me

Package Downloads

Package Source easyRNASeq_1.7.1.tar.gz
Windows Binary easyRNASeq_1.7.1.zip (32- & 64-bit)
Mac OS X 10.6 (Snow Leopard) easyRNASeq_1.7.1.tgz
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