@genebe/vesm_3b

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VESM-3B variant effect scores hg38

Labels: variant-effect protein-language-model missense
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README.md
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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
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.