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

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 <>
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="")

Try the DeepCNV package in your browser

Any scripts or data that you put into this service are public.

DeepCNV documentation built on May 2, 2019, 5:23 p.m.