DeepCNV: Exploiting Normal Contamination to Infer Copy Number from Deep Sequencing
Version 0.12.1

The DeepCNV package provides a systematic Bayesian framework for inferring copy number from deep sequencing data of one or a few genes.

Getting started

Package details

AuthorMark Zucker, Kevin R Coombes
MaintainerKevin Coombes <[email protected]>
LicenseApache License (== 2.0)
Package repositoryView on R-Forge
Installation Install the latest version of this package by entering the following in R:
install.packages("DeepCNV", repos="")

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DeepCNV documentation built on Aug. 17, 2017, 3:01 a.m.