chapmanb/delly
DELLY: Structural variant discovery by integrated paired-end and split-read analysis
Discovered public repositories for chapmanb in the GitHub catalog.
DELLY: Structural variant discovery by integrated paired-end and split-read analysis
Experiment: Clojure interface to ADAM distributed file formats for variants and aligned reads
a simple C++ library for parsing and manipulating VCF files, + many command-line utilities
a string to graph aligner
Idempotent, transactional runs of external command line programs
Homebrew repository for CloudBioLinux: incubator for formulas to end up in homebrew-science
Scientific formulae for the Homebrew package manager
Public repository.
a wee tool for random access into BGZF files.
Extended functionality for analyzing genomic variability, built on bcbio.variation and GATK
GATK Official Release Repository: contains the core MIT-licensed GATK framework, free for all uses
Content presented at the 2013 SciPy conference
build and test recipes for conda
Clojure API for Ensembl data access via JEnsembl
Investigate coverage metrics for variant calling experiments
A python library for interacting with CloudMan and Galaxy API
Official repository for IPython itself. Other repos in the IPython organization contain things like the website, documentation builds, etc.
Declarative data visualization in Clojure(Script).
Genome Connector: Clojure API to access multiple genomic resources
The gkno launcher for executing tools or pipelines
ClojureScript interface to Harvest's Chosen <select> library
Genetic changes we can believe in: a web based tool for variant visualization and analysis
Multimolecular NA Design tool with support for extensible sequence constraints
Access GenomeSpace data integration platform with simple Clojure API
Clojure library for interacting with Galaxy, CloudMan, and BioCloudCentral, built on blend4j
A fast Python library for VCF files leveraging Cython for speed.
a lightweight db framework for disease and population genetics.
Next-generation sequencing analysis pipelines built on Hadoop and Cascalog
Toolkit to analyze genomic variation data, built on the GATK with Clojure
Public repository.
CloudBioLinux: configure virtual (or real) machines with tools for biological analyses
Clojure web server providing full-text document searching via Lucene
In-progress code for various research projects
Exploring our genomic variability
Brad's fork of main repository
BioSQL web
Incubator for useful bioinformatics code, primarily in Python and R