saasCNV: Somatic Copy Number Alteration Analysis Using Sequencing and SNP Array Data
Version 0.3.4

Perform joint segmentation on two signal dimensions derived from total read depth (intensity) and allele specific read depth (intensity) for whole genome sequencing (WGS), whole exome sequencing (WES) and SNP array data.

Package details

AuthorZhongyang Zhang [aut, cre], Ke Hao [aut], Nancy R. Zhang [ctb]
Date of publication2016-05-18 02:04:56
MaintainerZhongyang Zhang <zhongyang.zhang@mssm.edu>
LicenseGPL (>= 2)
Version0.3.4
URL https://zhangz05.u.hpc.mssm.edu/saasCNV/
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("saasCNV")

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saasCNV documentation built on May 29, 2017, 10:10 a.m.