seqCNA: Copy number analysis of high-throughput sequencing cancer data
Version 1.22.0

Copy number analysis of high-throughput sequencing cancer data with fast summarization, extensive filtering and improved normalization

Package details

AuthorDavid Mosen-Ansorena
Bioconductor views CopyNumberVariation Genetics Sequencing
MaintainerDavid Mosen-Ansorena <dmosen.gn@cicbiogune.es>
LicenseGPL-3
Version1.22.0
Package repositoryView on Bioconductor
Installation Install the latest version of this package by entering the following in R:
source("https://bioconductor.org/biocLite.R")
biocLite("seqCNA")

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seqCNA documentation built on May 31, 2017, 3:27 p.m.