VarFish: comprehensive DNA variant analysis for diagnostics and research
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Updated
Nov 2, 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
VarFish REST API client (CLI + Python package)
Rust-based background worker for varfish-server
(Partial) port of biocommons/bioutils to Rust
VarFish (Snakemake) Client Workflow for Querying Snakemake
DEPRECATED Convert annotation database files to Var:fish: import format
Clinvar data builds for annonars
DEPRECATED, use https://github.com/bihealth/varfish-docker-compose instead
Automated evaluation of ACMG rules
Simple REST API wrapper for CADD-scripts
Repository for building IGSR data sets for use in VarFish
VarFish (Snakemake) Client Workflow for Validation
Re-implementation of the CADA phenotype-based prioritization algorithm
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