VarFish: comprehensive DNA variant analysis for diagnostics and research
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Updated
Sep 10, 2026 - Python
VarFish: comprehensive DNA variant analysis for diagnostics and research
VEP-like tool for sequence ontology and HGVS annotation of VCF files
A port of biocommons/hgvs to the Rust programming language
Genome annotation based on Rust and RocksDB
A port of biocommons/seqrepo to the Rust programming language
(Legacy) Annotate variants for import into VarFish server.
Download public databases for VarFish
Setup VarFish as using Docker Compose
Multi-source germline variant annotation pipeline
A method for predicting chromatin features and prioritizing non-coding rice variants using DNA language models.
VarFish REST API client (CLI + Python package)
Rust-based background worker for varfish-server
(Partial) port of biocommons/bioutils to Rust
Cembra Bio: evidence-governed research framework for universal genomic transfer models, with osteoarthritis variant prioritization as the reference application.
VarFish (Snakemake) Client Workflow for Querying Snakemake
DEPRECATED Convert annotation database files to Var:fish: import format
Simple REST API wrapper for CADD-scripts
Clinvar data builds for annonars
DEPRECATED, use https://github.com/bihealth/varfish-docker-compose instead
Personal profile repository for Vladimir Mitev, Founder and CEO of Helena Bioinformatics.
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