ga4gh-beacon / beacon-v2Links
Unified repository for the GA4GH Beacon v2 API standard
☆32Updated this week
Alternatives and similar repositories for beacon-v2
Users that are interested in beacon-v2 are comparing it to the libraries listed below
Sorting:
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- POC Nextflow pipeline to run Illumina DRAGEN software☆14Updated 5 months ago
- Python Phenopacket Tools☆15Updated 2 months ago
- GA4GH Variation Representation Python Implementation☆61Updated 3 weeks ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆34Updated 2 months ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆41Updated 3 years ago
- Pedigree drawing with ease☆24Updated 3 years ago
- An information model for representing variant annotations.☆26Updated 3 weeks ago
- Associations of genomic features, drugs and diseases☆48Updated 3 years ago
- [Alpha] Janis: an open source tool to machine generate type-safe CWL and WDL workflows☆44Updated 2 years ago
- Sphinx documentation source for a computational genomics tutorial.☆36Updated 5 years ago
- VCF-Miner: A graphical user interface for sorting, filtering and querying annotated VCF Files☆37Updated 6 years ago
- Repo for downloading and storing OMIM data☆19Updated 9 years ago
- Tibanna helps you run your genomic pipelines on Amazon cloud (AWS). It is used by the 4DN DCIC (4D Nucleome Data Coordination and Integr…☆71Updated 3 months ago
- GeneSCF moved to a dedicated GitHub page, https://github.com/genescf/GeneSCF☆20Updated 5 years ago
- Nextflow basic tutorial for newbie users☆33Updated 7 years ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆85Updated 3 weeks ago
- This repository contains Jupyter Notebooks containing GATK Best Practices Workflows☆26Updated 6 years ago
- Website to analyze conflicting assertions in ClinVar☆19Updated last week
- gnomAD browser pre-ASHG 2018☆33Updated 5 years ago
- A Nextflow Genome-Wide Association Study (GWAS) Pipeline☆36Updated 7 months ago
- JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes☆24Updated last year
- PharmGKB NGS Pipeline☆19Updated 7 years ago
- PathOS is a clinical application for filtering, analysing and reporting on NGS variants☆29Updated 4 years ago
- Create WDL documentation using Markdown.☆28Updated 2 months ago
- Research pipeline for exploring clinically relevant genomic variants☆16Updated this week
- a place for GA4GH-related wiki pages☆16Updated 8 years ago
- Collect of SO Ontologies☆102Updated 4 months ago
- CWL for GDC DNASeq workflows☆23Updated this week