MCP serverworld.sniff/sniff-mcp
Canine genomics for agents: breed allele frequencies, AI pathogenicity + OMIA clinical disease layer
Overview
Score?
UNRATED 0.672
of what a free look can see, on 30 looks
Looks
35
last 9 hr ago
Tools
18
More info
URL
mcp.sniff.world/mcp/
streamable-http
Says it is
Sniff 3.4.2
protocol 2025-06-18
In the record since
32 days ago
Among servers18,413 with a card
0median 0.606 · this server 0.672 · highest on record 0.8561
Toolsfrom sha256:4746f09c93…adf2cb
| Tool | Schema |
|---|---|
| ask Ask Sniff a natural-language canine-genetics question and get a GROUNDED, CITED answer (or an honest
abstain). Covers inherited diseases (OMIA) and their human homologs (the dog<-> |
input · output |
| ask_the_graph THE INSTRUMENT — ask a free-form CROSS-SPECIES genetics question and get FILTERED, HONEST HINTS (never a
confident guess). It compiles your question into a typed query plan over th |
input · output |
| ask_variant_context THE headline query. Given a CanFam4 position (e.g. '5:56189113'), return the variant's global +
popmax frequency, breed-stratified cross-breed frequencies, ESM2/Pangolin/phyloP pat |
input · output |
| breed_similarity Genetic distance between two breeds (top-10-PC Euclidean). Lower = more genetically similar. |
input · output |
| breed_summary Breed profile: top damaging common variants (ESM2<=-5 & breed AF>=5%), n_dogs, breed group.
Descriptive only — not a health ranking. |
input · output |
| breed_variant_frequency Breed-stratified allele frequency. Give a breed (e.g. 'bernese_mountain_dog') plus either a
variant position or a gene symbol. Returns AF (+ rank) for the variant, or per-variant A |
input · output |
| breeds_in_atlas List all 188 breeds with breed-stratified frequencies in the atlas. |
input · output |
| disease_bridge The fused OMIA disease layer as cited atoms. Give a `disease` (name or 'OMIA:001870-9615') for its
genes, inheritance, human homolog (OMIM/Mondo bridge), and variant pathogenicity |
input · output |
| disease_links A canine inherited disease (name or OMIA id) -> its governed OMIA clinical record: mode of inheritance,
causal gene(s), curated description (summary / clinical features / molecular |
input · output |
| disease_lookup Look up a canine inherited disease by name or OMIA id -> its governed OMIA clinical record (inheritance,
causal gene(s), curated description, clinical signs, human OMIM analog + Mo |
input · output |
| gene_summary Variants in a gene (by gene symbol), ranked by impact then ESM2 damage. Paginated (limit, default 25);
returns total_variants. Use af_min to filter by global AF. |
input · output |
| genes_indexed Top genes by number of variants in the atlas (discovery aid). |
input · output |
| metadata Atlas metadata: release, DOI, assembly, variant/breed counts, scope banner, and the RPC catalog. |
input · output |
| nearest_breeds Genetically nearest breeds to the given breed (top-10-PC Euclidean in canine genetic space).
Answers 'what breeds are most genetically similar to X?' via the PCA-256 breed co-embed |
input · output |
| search_diseases Search the canine disease catalogue by free text -> ranked candidates [{omia_id, disease, url, score}].
Use before disease_lookup when the exact name is unknown. Dog-only. |
input · output |
| semantic_search Faceted hybrid + semantic-ranker search over the whole knowledge base (diseases, breeds, Scout
discoveries). Use for fuzzy/thematic intent ('drug sensitivity in herding dogs', 'bre |
input · output |
| variant_lookup Single-variant lookup by CanFam4 position: ref/alt, global + popmax AF, consequence, gene,
ESM2/Pangolin/phyloP, deleteriousness tier, canonical URL, provenance. |
input · output |
| variant_search Filtered discovery over all 9.67M variants. Predicates (combine freely): esm_max (ESM2 LLR <=),
phylop_min (phyloP >=), popmax_min (popmax AF >=), gene_in (list of gene symbols), c |
input · output |
Verify it yourself
npx teppi-check https://mcp.sniff.world/mcp/curl -s https://api.teppi.xyz/v1/trust/mcp/mcs_01M1FZ2R2Y5N7J56TZAYYDFFAG