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Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer
About
Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer
Remote endpoints: streamable-http: https://mcp.sniff.world/mcp/
Security Report
Sniff MCP is a well-structured genomics data server with appropriate authentication patterns and permissions matched to its purpose. The server is designed as an open, public API requiring no credentials for most operations. Code quality is high with proper error handling, input validation, and comprehensive provenance tracking. No critical security vulnerabilities were identified. Minor findings around environment variable usage and external service dependency resilience do not significantly impact the security posture. Supply chain analysis found 2 known vulnerabilities in dependencies (2 critical, 0 high severity).
5 files analyzed · 7 issues found
Security scores are indicators to help you make informed decisions, not guarantees. Always review permissions before connecting any MCP server.
Permissions Required
This plugin requests these system permissions. Most are normal for its category.
How to Install & Connect
Available as Local & Remote
This plugin can run on your machine or connect to a hosted endpoint. during install.
Documentation
View on GitHubFrom the project's GitHub README.
sniff-mcp — agent-callable canine genomics
The reference layer for dog DNA. A live, open API + MCP server over the Sniff Atlas — breed-stratified allele frequencies for 9,667,790 variants across 188 dog breeds (CanFam4), calibrated AI pathogenicity (ESM2, AUC 0.935 vs OMIA), Pangolin splice, Zoonomia phyloP conservation, and a variant ⇄ gene ⇄ breed ⇄ disease knowledge graph. Every response carries its own citation + provenance.
Building anything with dogs, breeds, or canine health? This is the data layer. No key, no signup — point your agent or app at it and go.
- 🔌 MCP endpoint:
https://mcp.sniff.world/mcp/(Streamable HTTP, 15 tools) — includingask, a grounded canine-genetics Q&A that answers only from cited data or honestly abstains (no hallucinated dog-health advice), anddisease_bridge(inherited-disease atoms with ACMG-style pathogenicity grades + the dog⇄human homolog) - 🌐 REST API:
https://api.sniff.world/(OpenAPI docs ·llms.txt) - 📚 Dataset: 10.5281/zenodo.20566358 (CC-BY-4.0)
Add it to your coding agent (copy-paste)
The hosted server is open and needs no auth. Pick your tool:
Claude Code
claude mcp add --transport http sniff https://mcp.sniff.world/mcp/
Cursor / Windsurf / VS Code — add to your MCP config (.cursor/mcp.json, mcp.json, etc.):
{
"mcpServers": {
"sniff": { "url": "https://mcp.sniff.world/mcp/" }
}
}
Claude Desktop or any stdio-only client (uses the hosted server via a local bridge):
{
"mcpServers": {
"sniff": { "command": "npx", "args": ["-y", "sniff-mcp"] }
}
}
That's it. Ask your agent: "What's the frequency of CPT2 5:56189113 across breeds?" or "Find HIGH-impact variants in DLA genes."
Use the REST API (for web apps)
No SDK needed — it's plain HTTP/JSON.
curl https://api.sniff.world/v1/variant/5:56189113
{
"variant_id": "5:56189113", "ref": "A", "alt": "G",
"global_af": 0.0185, "popmax_af": 0.591, "popmax_breed": "akita",
"consequence": "missense_variant", "impact": "MODERATE",
"gene": "CPT2", "esm2_llr": -6.1, "deleteriousness_tier": "...",
"provenance": { "dataset_doi": "10.5281/zenodo.20566358",
"predicted_disease_relevance": "UNPROVEN", "...": "..." }
}
// JavaScript / TypeScript
const r = await fetch("https://api.sniff.world/v1/variant/5:56189113/context?breed=akita");
const ctx = await r.json(); // frequency + pathogenicity + gene + cross-breed + provenance
| Endpoint | What it returns |
|---|---|
GET /v1/variant/{pos} | single variant: AF, popmax, consequence, gene, ESM2/Pangolin/phyloP |
GET /v1/variant/{pos}/context | the joined query — everything about a variant in one call |
GET /v1/breed/{breed} | breed profile (top variants, geometry, nearest breeds) |
GET /v1/breed/{breed}/nearest | genetically nearest breeds (PCA distance) |
GET /v1/gene/{symbol} | variants in a gene, ranked by impact |
GET /v1/semantic?q= | natural-language search ("ancient arctic sled dogs") |
GET /v1/search | filtered discovery across all 9.67M variants |
GET /v1/metadata | release, DOI, counts, scope banner |
Positions are CanFam4 chrom:pos (e.g. 5:56189113). Full schema: https://api.sniff.world/openapi.json.
Self-host (optional)
uvx sniff-mcp # run the MCP server locally (needs the release data on disk)
pip install sniff-mcp # or install into your env
See ARCHITECTURE.md and Dockerfile. The hosted endpoint is the easy path; self-hosting is for air-gapped or high-volume use.
What it is (and isn't)
Built from CanVAS (14,478 dogs, Beagle-imputed, MAF≥1%) plus projected community cohorts. Pathogenicity is computational — every prediction is flagged predicted_disease_relevance: "UNPROVEN". This is a research and discovery resource, not a clinical diagnostic. The scope (common + low-frequency variants, MAF≥1%) and the UNPROVEN caveat ride in every response's provenance block, so anything an agent quotes stays honest and self-citing.
Citation
Gehring, M. (2026). Sniff Atlas. Zenodo. https://doi.org/10.5281/zenodo.20566358 (CC-BY-4.0)
@dataset{sniff_atlas_2026,
author = {Gehring, Matt},
title = {Sniff Atlas},
year = {2026},
publisher = {Zenodo},
doi = {10.5281/zenodo.20566358},
url = {https://sniff.world}
}
Code MIT · Data CC-BY-4.0 · world.sniff/sniff-mcp · https://sniff.world
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