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

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 <[email protected]>
LicenseGPL-3
Version1.28.0
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 Nov. 1, 2018, 3:50 a.m.