PSCBS: Analysis of Parent-Specific DNA Copy Numbers

Segmentation of allele-specific DNA copy number data and detection of regions with abnormal copy number within each parental chromosome. Both tumor-normal paired and tumor-only analyses are supported.

Package details

AuthorHenrik Bengtsson [aut, cre, cph], Pierre Neuvial [aut], Venkatraman E. Seshan [aut], Adam B. Olshen [aut], Paul T. Spellman [aut], Richard A. Olshen [aut], Frank E Harrell Jr [ctb] (Weighted quantile estimator adopted from Hmisc::wtd.quantile())
Bioconductor views CopyNumberVariants Genetics Microarray OneChannel SNP TwoChannel aCGH
MaintainerHenrik Bengtsson <henrikb@braju.com>
LicenseGPL (>= 2)
Version0.66.0
URL https://github.com/HenrikBengtsson/PSCBS
Package repositoryView on CRAN
Installation Install the latest version of this package by entering the following in R:
install.packages("PSCBS")

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PSCBS documentation built on Oct. 23, 2021, 9:09 a.m.