szilvajuhos/sarek.pathfindr: Scoring somatic and germline variants for cancer genome analysis

Sarek is workflow to analyse NGS data, to obtain and annotate SNPs, indels and structural variants from tumour/normal samples. This module is to score and rank these variants

Getting started

Package details

Maintainer
LicenseMIT
Version0.0.0.9000
Package repositoryView on GitHub
Installation Install the latest version of this package by entering the following in R:
install.packages("remotes")
remotes::install_github("szilvajuhos/sarek.pathfindr")
szilvajuhos/sarek.pathfindr documentation built on Dec. 19, 2020, 3:13 a.m.