Alphagenome
Looks up precomputed AlphaGenome Atlas effects for any GRCh38 single-nucleotide variant...
Install
npx skills add K-Dense-AI/scientific-agent-skills --skill alphagenome -g -a claude-code -y- Repository
- K-Dense-AI/scientific-agent-skills55.7k
- Category
- Design
- Updated
- 9d ago
- License
- MIT
- Context cost
- Mediumabout 3,000 tokens
- Runs scripts
- Yes, review before use
What it does
Looks up precomputed AlphaGenome Atlas effects for any GRCh38 single-nucleotide variant (AVI score with Phred and 18 SHAP feature attributions, plus raw and quantile scores for RNA-seq, DNase, ATAC, ChIP-TF, ChIP-histone, CAGE, PRO-cap, splicing, polyadenylation and contact-map tracks), scores variants or scans windows on demand with the AlphaGenome model for human and mouse (variant scoring, in silico mutagenesis, REF-versus-ALT track prediction), and builds Atlas website deep links. Use when the user mentions AlphaGenome, AlphaGenome Atlas, AVI or AlphaGenome Variant Impact, DeepMind variant effect prediction, or wants to prioritise or mechanistically interpret non-coding, regulatory, splicing, enhancer, promoter, or chromatin-accessibility effects of SNVs from a VCF, credible set, or region. Research use only; not a clinical tool.
AlphaGenome and the AlphaGenome Atlas
AlphaGenome is DeepMind's sequence-to-function model: 1 Mb of DNA in,
predictions at modality-specific resolutions for eleven assay types across
thousands of human and mouse tracks out. The AlphaGenome Atlas (released 2026-09-08) is that model run once over
every possible single-nucleotide change in GRCh38, about 9 billion variants,
stored with a single ranking number, the AlphaGenome Variant Impact (AVI)
score, its genome-wide percentile, and an 18-way attribution of what drives it.
Both are reached through one pip install alphagenome and one API key.
Research and theoretical modelling only. API outputs must not be used to train other models, and are not for diagnostic procedures or medical decisions. Permissive-use downloads have separate terms; check the artifact licence.
When to use which
| You have | Use | Why |
|---|---|---|
| hg38 SNVs (a VCF, a credible set, a region up to ~1 kb) | Atlas via scripts/atlas_query.py | precomputed, higher quota, includes AVI and attributions |
| indels, mouse variants, a non-reference background, a custom scorer or window | model via scripts/score_variants.py or Python | the Atlas is SNV-only and hg38-only |
| a hypothesis to explain (which motif, which tissue, REF vs ALT tracks) | model predict_variant + plots, Atlas track scores, portal link | mechanism, not just rank |
| GRCh37 coordinates, rsIDs, unnormalised indels | genomic-coordinates first, then come back | wrong build or swapped REF gives a plausible wrong answer |
| ClinVar assertions, gene-disease validity, ACMG framing | folklore-variant-evidence, database-lookup | AlphaGenome is one evidence line, never the verdict |
| promoter/enhancer/expression predictions without a DeepMind key | genomic-intelligence | different provider, keyless demo tier |
