simexin's Stars
Illumina/hap.py
Haplotype VCF comparison tools
Lasagne/Lasagne
Lightweight library to build and train neural networks in Theano
mozack/abra
Assembly Based ReAligner
gt1/biobambam2
Tools for early stage alignment file processing
ytdl-org/youtube-dl
Command-line program to download videos from YouTube.com and other video sites
bcbio/bcbio-nextgen
Validated, scalable, community developed variant calling, RNA-seq and small RNA analysis
atks/vt
A tool set for short variant discovery in genetic sequence data.
scikit-learn/scikit-learn
scikit-learn: machine learning in Python
tensorflow/tensorflow
An Open Source Machine Learning Framework for Everyone
mutalyzer/mutalyzer2
HGVS variant nomenclature checker
counsyl/hgvs
HGVS variant name parsing and generation
XX-net/XX-Net
A proxy tool to bypass GFW.
vcftools/vcftools
A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.
arq5x/bedtools2
bedtools - the swiss army knife for genome arithmetic
genome/genome
Core modules used by the GMS
freebayes/freebayes
Bayesian haplotype-based genetic polymorphism discovery and genotyping.
Bash-it/bash-it
A community Bash framework.
christoomey/vim-tmux-navigator
Seamless navigation between tmux panes and vim splits
genome/gms
The Genome Modeling System installer
adamewing/bamsurgeon
tools for adding mutations to existing .bam files, used for testing mutation callers
samtools/hts-specs
Specifications of SAM/BAM and related high-throughput sequencing file formats
broadgsa/gatk-protected
Official code repository for GATK versions 1.0 through 3.7 (full licensed package). For GATK 4 code, see the https://github.com/broadinstitute/gatk repository
samtools/bcftools
This is the official development repository for BCFtools. See installation instructions and other documentation here http://samtools.github.io/bcftools/howtos/install.html
samtools/htslib
C library for high-throughput sequencing data formats
samtools/samtools
Tools (written in C using htslib) for manipulating next-generation sequencing data
broadinstitute/picard
A set of command line tools (in Java) for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF.
broadgsa/gatk
Official code repository for GATK versions 1.0 through 3.7 (core engine). For GATK 4 code, see the https://github.com/broadinstitute/gatk repository
broadinstitute/mutect
MuTect -- Accurate and sensitive cancer mutation detection
broadinstitute/xtermcolor
Python library for terminal color support (including 256-color support)
broadinstitute/gatk
Official code repository for GATK versions 4 and up