NGScopy: NGScopy: Detection of Copy Number Variations in Next Generation Sequencing sequencing
Version 1.10.0

NGScopy provides a quantitative caller for detecting copy number variations in next generation sequencing (NGS), including whole genome sequencing (WGS), whole exome sequencing (WES) and targeted panel sequencing (TPS). The caller can be parallelized by chromosomes to use multiple processors/cores on one computer.

Package details

AuthorXiaobei Zhao [aut, cre, cph]
Bioconductor views CopyNumberVariation DNASeq ExomeSeq Sequencing TargetedResequencing WholeGenome
MaintainerXiaobei Zhao <xiaobei@binf.ku.dk>
LicenseGPL (>=2)
Version1.10.0
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("NGScopy")

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NGScopy documentation built on May 31, 2017, 11:19 a.m.