DeepCNV: Exploiting Normal Contamination to Infer Copy Number from Deep Sequencing
Version 0.12.2

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
Date of publication2018-05-19 12:43:04
MaintainerKevin Coombes <[email protected]>
LicenseApache License (== 2.0)
Version0.12.2
URL http://oompa.r-forge.r-project.org/
Package repositoryView on R-Forge
Installation Install the latest version of this package by entering the following in R:
install.packages("DeepCNV", repos="http://R-Forge.R-project.org")

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DeepCNV documentation built on May 19, 2018, 3 p.m.