vincent-dk/epiG: Statistical Inference of Epi-Allelic Patterns from Whole-Genome Bisulphite Sequencing Data
Version 0.9.0

Statistical method to infer epiallelic haplotypes, annotated with CpG methylation marks and polymorphisms, from whole genome bisulphite sequencing data, and nucleosome occupancy from NOMe-seq data.

Getting started

Package details

AuthorMartin Vincent
MaintainerMartin Vincent <[email protected]>
LicenseGPL (>= 2)
Version0.9.0
URL
Package repositoryView on GitHub
Installation Install the latest version of this package by entering the following in R:
install.packages("devtools")
library(devtools)
install_github("vincent-dk/epiG")
vincent-dk/epiG documentation built on May 27, 2017, 8:53 p.m.