navinlabcode/copykat: COPYKAT: Inference of genomic copy number and subclonal structure of human tumors from high-throughput single cell RNA-seq data

COPYKAT is a computational tool using integrative Bayesian approaches to identify genome-wide aneuploidy at 5MB resolution in single cells to separate aneuploid (tumor) cells from diploid (normal) cells, and tumor subclones using high-throughput sc-RNAseq data.

Getting started

Package details

AuthorRuli Gao
MaintainerRuli Gao <ruli.gao@northwestern.edu>
LicenseGPL-2
Version1.1.0
Package repositoryView on GitHub
Installation Install the latest version of this package by entering the following in R:
install.packages("remotes")
remotes::install_github("navinlabcode/copykat")
navinlabcode/copykat documentation built on June 29, 2024, 2:31 a.m.