easyRNASeq: Count summarization and normalization for RNA-Seq data
Version 2.12.1

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.

Package details

AuthorNicolas Delhomme, Ismael Padioleau, Bastian Schiffthaler, Niklas Maehler
Bioconductor views GeneExpression Genetics Preprocessing RNASeq
MaintainerNicolas Delhomme <[email protected]>
Package repositoryView on Bioconductor
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easyRNASeq documentation built on July 15, 2017, 2 a.m.