easyRNASeq (version 2.8.2)

Count summarization and normalization for RNA-Seq data

Description

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.

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Version

2.8.2

License

Artistic-2.0

Last Published

March 10th, 2015

Functions in easyRNASeq (2.8.2)