jdiez/vcfnp
Load numpy arrays from VCF (variant call file)
Discovered public repositories for jdiez in the GitHub catalog.
Load numpy arrays from VCF (variant call file)
Simpsons characters in pure CSS
Tools for next-generation sequencing analysis
matplotlib: plotting with Python
Rails frontend to The Genome Institute's drug gene interaction database.
Specifications of SAM/BAM and related high-throughput sequencing file formats
VCF Importer: Converts a VCF file into a Variants GTable object
Easily create HTML, spreadsheet, or PDF tables from common Python data sources
Awesome web-browseable Web APIs.
Infrastructure code to support DNA pipeline
Filtering and Annotation of Variants that are Rare
Python wrapper -- and more -- for Aaron Quinlan's BEDTools (bioinformatics tools)
a simple C++ library for parsing and manipulating VCF files, + many command-line utilities
Toolkit for processing sequences in FASTA/Q formats
A library and collection of scripts to work with Illumina paired-end data (for CASAVA 1.7+ pipeline).
Simple job queues for Python
A Variant Call Format reader for Python.
a lightweight db framework for disease and population genetics.
GATK Official Release Repository: contains the core MIT-licensed GATK framework, plus "protected" tools restricted to non-commercial use only
python utilities to work with Variant Call Format files (VCF)
Quantitative Insights Into Microbial Ecology (QIIME): Official repository for software and unit tests
Official git repository for Biopython (converted from CVS)
Useful bioinformatics code, primarily in Python and R