Wellcome Trust Sanger Institute - Human Genetics Informatics's Projects
Docker and Docker Machine wrapper scripts for OS X
Converts CWL Inline Javascript expressions into explicit processing steps
I don't care how it's done, I just want to use it in my tests!
A collection of scripts for evaluating variant callers
A tool to give reports on what Vault will delete when we launch it on a project directory
A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.
Docker image for VEP which supports Loftee Plugin
A Robust tool for estimation of DNA contamination and genetic ancestry from sequence reads
tools for working with variant graphs
The overall codebase developed and used by the Vertebrate Resequencing group at the Sanger Institute (HGI edition)
Generic pipeline system
Runner pipelines
A web frontend for Arboretum
Convert Workflow Definiton Language (WDL) to CWL
Browser-based Shiny frontend to view internal Lustre volume reports
The web front end for ShareLaTeX, a web-based collaborative LaTeX editor
A system that accepts incoming webhooks from the Internet and routes them to internal locations, depending on a configuration that can be dynamically modified by users
A flexible WSGI implementation and toolkit (unofficial fork)
WINGS Workflow System
Github webpage for HGI projects
Tools to view LSF hierarchical fairshare UserGroup shares and current priority (e.g. in a treemap)
Open source tool for working with XAD files
Bearer token codec
Generate secure multiword passwords/passphrases, inspired by XKCD
Yet Another OpenStack Ansible Dynamic Inventory Script
scRNA multimodal analysis pipeline utilised for large dataset processing