Ensembl/VEP_plugins

The Ensembl Variant Effect Predictor predicts the functional effects of genomic variants

Python interface to access reference genome features (such as genes, transcripts, and exons) from Ensembl

Documentation for the ANNOVAR software

A modular annotation tool for genomic variants

This API provides programmatic access to the AlphaGenome model developed by Google DeepMind.

Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).

VCF visualization interface

🦖 ClawBio - The first bioinformatics-native AI agent skill library. Local-first. Reproducible. Open. Free.

Python application to generate self-contained pages embedding IGV visualizations, with no dependency on original input files.