Count summarization and normalization for RNA-Seq data.

Bioconductor version: Release (2.11)

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:


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



PDF R Script RNA-Seq
PDF   Reference Manual
Text   NEWS


biocViews GeneExpression, Genetics, Preprocessing, RNAseq, Software
Version 1.4.2
In Bioconductor since BioC 2.10 (R-2.15)
License Artistic-2.0
Depends graphics, methods, parallel, utils, genomeIntervals(>= 1.14.0), Biobase(>= 2.18.0), BiocGenerics(>= 0.4.0), biomaRt(>= 2.14.0), edgeR(>= 3.0.0), Biostrings(>= 2.26.0), BSgenome(>= 1.26.0), DESeq(>= 1.10.0), GenomicRanges(>= 1.10.0), IRanges(>= 1.16.0), Rsamtools(>= 1.10.0), ShortRead(>= 1.16.0)
Suggests BSgenome.Dmelanogaster.UCSC.dm3(>= 1.3.17), GenomicFeatures(>= 1.10.0), RnaSeqTutorial(>= 0.0.10)
System Requirements
Depends On Me RnaSeqTutorial
Imports Me
Suggests Me

Package Downloads

Package Source easyRNASeq_1.4.2.tar.gz
Windows Binary easyRNASeq_1.4.2.zip (32- & 64-bit)
MacOS 10.5 (Leopard) easyRNASeq_1.4.2.tgz
Package Downloads Report Download Stats

Mailing Lists »

Post questions about Bioconductor packages to our mailing lists. Read the posting guide before posting!

Fred Hutchinson Cancer Research Center