@genebe/gpn-star-hg38-m447-200m

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GPN-Star (mammals, 200M) - genome-wide variant effect log-likelihood ratio

Labels: variant-impact conservation deep-learning gpn-star
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About gpn-star-hg38-m447-200m

GPN-Star (mammals, 200M) — genome-wide variant effect scores

This annotation contains exhaustive genome-wide single-nucleotide variant scores from GPN-Star, a genomic language model from the Song Lab, for the human reference genome (GRCh38). This specific model (songlab/gpn-star-hg38-m447-200m) was trained on a whole-genome alignment of 447 mammalian species and has 200M parameters.

Every possible single-nucleotide substitution at every position of the genome is scored with two columns:

  • llr_calibrated: calibrated log-likelihood ratio for the specific reference-to-alternate substitution.
  • abs_llr_calibrated: a separately calibrated score from the model. Despite its name, it is not the absolute value of llr_calibrated.

Refer to the source publication for the exact calibration methodology and the sign convention of both scores.

Citation

Ye C, Benegas G, Albors C, Li JC, Prillo S, Fields PD, Clarke B, Song YS. Predicting genome-wide functional constraints with GPN-Star. Nature. 2026. https://www.nature.com/articles/s41586-026-11005-5

Preprint: https://www.biorxiv.org/content/10.1101/2025.09.21.677619v1

Code: https://github.com/songlab-cal/gpn

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, 08:10:25 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.