@genebe/vesm_3b
Latest release Active PublicVESM-3B variant effect scores hg38
About vesm_3b
This annotation is derived from the VESM-3B hg38 precomputed variant-effect scores. It retains the source score named VESM (3B) under vesm_3b and maps variants to SPDI keys. If multiple source rows map to one genomic allele, the minimum score is retained.
The VESM models and precomputed predictions are described in:
Dinh T, Jang S-K, Zaitlen N, Ntranos V. Compressing the collective knowledge of ESM into a single protein language model. Nature Methods. 2026;23:772–784. doi:10.1038/s41592-026-03050-9. Please cite the paper when using these scores.
The VESM score files describe predicted variant effects; the score is preserved as supplied and is not recalibrated by this builder.
Genome Reference & Assembly
This database is compiled for homo_sapiens using reference assembly GRCh38.
Metadata & Attributes
- Maintainer / Owner @genebe
- Database Type Variant Annotation
- Genome Assembly homo_sapiens (GRCh38)
- License MIT License
- Created Date 24 Sept 2026, 14:50:30 UTC