broadinstitute/inferCNV: Infer Copy Number Variation from Single-Cell RNA-Seq Data

Using single-cell RNA-Seq expression to visualize CNV in cells.

Getting started

Package details

Bioconductor views Bayesian CopyNumberVariation Genetics GenomicVariation HiddenMarkovModel SingleCell Software StatisticalMethod StructuralVariation Transcriptomics VariantDetection
Maintainer
LicenseBSD_3_clause + file LICENSE
Version1.3.1
URL https://github.com/broadinstitute/inferCNV/wiki
Package repositoryView on GitHub
Installation Install the latest version of this package by entering the following in R:
install.packages("remotes")
remotes::install_github("broadinstitute/inferCNV")
broadinstitute/inferCNV documentation built on Nov. 19, 2019, 5:13 a.m.