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 <dmosen.gn@cicbiogune.es>
LicenseGPL-3
Version1.36.0
Package repositoryView on Bioconductor
Installation Install the latest version of this package by entering the following in R:
if (!requireNamespace("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("seqCNA")

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seqCNA documentation built on Nov. 8, 2020, 7:09 p.m.