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

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]
MaintainerZhongyang Zhang <>
LicenseGPL (>= 2)
Package repositoryView on CRAN
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saasCNV documentation built on May 1, 2019, 7:49 p.m.