Skip to content

This repository (currently work in progress) is used to store the code and findings exploring genomic causes of Unexplained Familial Cancer.

License

Notifications You must be signed in to change notification settings

vanallenlab/unexplained_familial_cancer

Folders and files

NameName
Last commit message
Last commit date

Latest commit

 

History

36 Commits
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Repository files navigation

The Unexplained Familial Cancer Project

Variant Calling from germline whole-genome sequencing (WGS) across cancer types

Copyright (c) 2023-Present, Ryan L. Collins, Noah Fields, and the Van Allen, Gusev, and Haigis laboratories at Dana-Farber Cancer Institute. Distributed under terms of the GNU GPL v2.0 License (see LICENSE).

Note: this repository is under active development. More documentation will be added as the project evolves.


Synopsis

This repository contains the working code and scripts used to detect, genotype, filter, and annotate germline variants from germline WGS across cancer types. This code also contains code to analyze and graph results.


Table of Contents

Directory Description
docker/ Instructions for building project-related Docker images
refs/ Reference .jsons and dotfiles
scripts/ Stand-alone scripts called by various workflows
shell/ Shell snippets for running specific processes or analyses
src/ Source code for the g2cpy and G2CR companion libraries
wdl/ Stand-alone WDL workflows

About

This repository (currently work in progress) is used to store the code and findings exploring genomic causes of Unexplained Familial Cancer.

Resources

License

Stars

Watchers

Forks

Releases

No releases published

Packages

No packages published

Languages