genome/sciclone-meta
accessory scripts and documentation related to the sciclone R package at genome/sciclone
Discovered public repositories for genome in the GitHub catalog.
accessory scripts and documentation related to the sciclone R package at genome/sciclone
Puppet module for managing PostgreSQL
Client-facing API for the PTero system
Rich Transactional Objects for Perl
Public repository.
Public repository.
Petri net core of the PTero system
Examine active users with this mcollective RPC agent.
Design documents for the PTero services
Perl client for the nessy-server lock daemon
Provide access to various genome services such as procera, amber, and others.
Ptero services to run shell commands
Public repository.
Public repository.
Public repository.
Example Data for SomaticSniper
Public repository.
Public repository.
Public repository.
Create JIRA issues when keywords are matched in RSS feeds.
Analyze exome data for Mendelian disorders. Still in alpha-testing.
The Genome Modeling System installer
R package that uses a variational Bayesian approach to fitting a mixture of Beta distributions
Pindel can detect breakpoints of large deletions, medium sized insertions, inversions, tandem duplications and other structural variants at single-based resolution from next-gen sequence data. It uses a pattern growth approach to identify the breakpoints of these variants from paired-end short reads.
A fork of chimerascan that supports variable read lengths
An R package for inferring the subclonal architecture of tumors
Autoloading configuration manager for use in the genome modeling system
Mirror of internal repository for TestTracker.
simple static plots of read pairing information
in-progress port of our webviews to rails
the workflow server used at TGI
Barebones debian files to make a passenger deb.
iBWA is a fork of Heng Li's BWA aligner with support for iteratively adding alternate haplotypes, reference patches, and variant hypotheses.
Count bases in BAM/CRAM files
Public repository.
This is a python command line client for Atlassian's Jira issue tracker.
Graphite Config and Cron Scripts
An approximate sequence pattern matcher for FASTQ/FASTA files.
A tool to call somatic single nucleotide variants.
common build scripts used in c/c++ projects
a tool for processing .bed and .vcf files
extract 454 Genome Sequencer reads from a SFF file and convert them into a FASTQ formatted output
custom tab−completion for Perl apps
SV detection from paired end reads mapping
Washington University Genome Center Hudson testing suite and deploy scripts