ga4gh / wikiLinks
a place for GA4GH-related wiki pages
☆16Updated 8 years ago
Alternatives and similar repositories for wiki
Users that are interested in wiki are comparing it to the libraries listed below
Sorting:
- Convert CWL to WDL☆17Updated 8 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆29Updated 3 months ago
- Import a CWL workflow specification to Nextflow script (experimental)☆27Updated 7 years ago
- Annotation of VCF variants with functional impact and from databases (executable+library)☆62Updated last month
- CWL for GDC DNASeq workflows☆22Updated last month
- [Experimental] Workflow Definition Language (WDL) to CWL☆28Updated 3 years ago
- CWL CommandLineTool descriptions for biology/life-sciences related applications☆79Updated 5 months ago
- conda recipes for genomic data☆84Updated 4 years ago
- A repository for the schemas used for the Data Repository Service.☆63Updated last month
- Workflows used for WGS data processing -- replaced by https://github.com/gatk-workflows/gatk4-genome-processing-pipeline☆57Updated 5 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- Variant Calling Pipeline in Cromwell/WDL☆22Updated 5 years ago
- GA4GH Variation Representation Python Implementation☆60Updated 3 weeks ago
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- gnomAD browser pre-ASHG 2018☆33Updated 4 years ago
- hail-based pipelines for annotating variant callsets and exporting them to elasticsearch☆23Updated this week
- [Alpha] Janis: an open source tool to machine generate type-safe CWL and WDL workflows☆45Updated 2 years ago
- VarSim: A high-fidelity simulation validation framework for high-throughput genome sequencing with cancer applications☆89Updated 11 months ago
- Collect of SO Ontologies☆101Updated last week
- Aligner for sequencing data☆21Updated 9 years ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago
- Whole Genome Sequenceing Structural Variation Pipelines☆17Updated 6 years ago
- ☆82Updated 3 years ago
- Testing building mulled containers for multi-requirement tools.☆78Updated last week
- Thousand Variant Callers Project Repository☆73Updated 5 years ago
- Bioinformatics tool outputs converter to JSON or YAML☆35Updated 3 months ago
- H3ABioNet 16S rDNA diverstity analysis package☆19Updated 6 years ago
- Extensible specification for representing and uniquely identifying biological sequence variation☆93Updated last month
- Nextflow workshop 2018 -- Training pages -> https://nextflow-io.github.io/nf-hack18/☆18Updated 6 years ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆83Updated last month