Внимание медгенетикам - альфагеном выложил скоры для 9 миллиардов геномных вариантов. Доступ по API

https://deepmind.google.com/science/alphagenome/atlas

AlphaGenome Atlas is an integrated data resource that predicts the functional impact of all 9 billion possible single nucleotide variants (SNVs) across the human genome. By unifying coding and non-coding predictive models, it streamlines the prioritisation and interpretation of variants.

Unified Variant impact scoring: Combines coding and non-coding predictions into a single, standardized AlphaGenome Variant Impact (AVI) score.
Genome-wide scale: Access precomputed variant effect predictions spanning the entire human genome.
Zero-code exploration: Spot-check individual variants and dive into granular genomic context directly in your browser.
Seamless agentic integration: Connect effortlessly with AI agent workflows to scale analyses and transition to Atlas website visualisations.

More details:
- 🌐 Portal: https://lnkd.in/gEd_9YjY
- 🎥 Video: https://lnkd.in/gjCs3y6F
- 📖 Blog: https://lnkd.in/gdBM4D7T
- 📄 Preprint: https://lnkd.in/gt2pQeZv
- 🧬 Motif heatmap: https://lnkd.in/gn826x7c