Mavedb Link
БесплатноНе проверенMCP server for MaveDB: quantitative variant-effect scores from Multiplexed Assays of Variant Effect (MAVE) and deep mutational scanning — functional evidence as
Описание
MCP server for MaveDB: quantitative variant-effect scores from Multiplexed Assays of Variant Effect (MAVE) and deep mutational scanning — functional evidence as typed tools for LLM agents.
README
Python 3.12+ CI Conformance License: MIT
A read-only Model Context Protocol (MCP) server, built on FastMCP 3.x, that grounds
variant-effect work in MaveDB — the database of Multiplexed Assays
of Variant Effect, which assigns quantitative functional scores to variants by deep mutational
scanning and related assays. Part of the GeneFoundry *-link fleet; federates into
genefoundry-router under the mavedb
namespace.
[!IMPORTANT] Research use only. Not clinical decision support. Do not use for diagnosis, treatment, triage, or patient management.
Why
MaveDB's REST API hands back a score and its interpretation as separate, unjoined parts of the record. The scores arrive as a CSV column of bare floats; whether a given float means abnormal depends on that score set's own curated calibration ladder, which lives elsewhere in the record and which the caller must fetch and apply by hand. A raw MAVE score is uninterpretable on its own, and an agent handed one will either guess or hallucinate a threshold.
This server never returns a naked score. It carries MaveDB's curated interpretation layer —
functional-classification thresholds with ACMG PS3/BS3 evidence strength and OddsPath ratios —
alongside every value, and resolves identifiers (HGVS, GA4GH VRS, URN) internally instead of
forcing a map-first round-trip. find_variant answers the question the record-oriented API
leaves you to assemble yourself: what does every MAVE dataset say about this one variant?
Reads are served from a local SQLite mirror of the CC0 Zenodo bulk dump and fall back to the live API on a miss, so lookups are fast and work offline.
Quick start
Hosted — no install required:
claude mcp add --transport http mavedb-link https://mavedb-link.genefoundry.org/mcp
Or run it locally (Python 3.12+, uv):
uv sync --group dev
uv run python server.py --transport unified --host 127.0.0.1 --port 8000
curl -s localhost:8000/health | python -m json.tool
claude mcp add --transport http mavedb-link http://127.0.0.1:8000/mcp
No data build is required — the server runs pure-live out of the box. Building the local mirror is optional, and makes lookups fast and offline:
make data-build # download the latest Zenodo dump → data/mavedb.sqlite
--transport unified serves REST and MCP at /mcp; --transport http is REST/health only
and exposes no MCP endpoint — router and MCP clients need unified. For Claude Desktop
(stdio), run uv run python mcp_server.py instead.
Tools
| Tool | Purpose |
|---|---|
search_score_sets |
Full-text + faceted search of score sets (gene, organism, author, journal, keyword) |
get_score_set |
Score-set record (targets, publications, licence) + score_calibrations: ACMG/OddsPath thresholds |
get_variant_scores |
The quantitative variant × score table (paged); each row carries its calibrated functional class |
get_variant_score |
One variant's score + per-calibration classification (by variant URN, or score-set URN + HGVS) |
get_classified_variants |
Every variant in a calibrated functional class (e.g. all abnormal / PS3), with scores |
get_score_distribution |
Server-side summary stats (quartiles, histogram) + a query score's percentile and class |
find_variant |
One variant's score + class across every score set — anchored by GA4GH VRS id, variant_urn, or a bare hgvs= (+ optional gene_symbol=) resolved to VRS internally |
get_hgvs_validation |
Validate an HGVS string and surface why it is invalid (reference mismatch, missing accession) |
get_gene_score_sets |
All published MAVE datasets for an HGNC gene symbol (lean listing with a has_calibrations flag) |
get_experiment |
Experiment record + child score-set URNs |
search_experiments |
Full-text experiment search |
get_mapped_variants |
Genome-mapped GA4GH VRS alleles + ClinGen Allele IDs for a score set |
get_collection |
Curated collection members (URN from a score set's official_collections, or mavedb.org) |
get_server_capabilities |
Discovery surface: tools, signatures, limits, error taxonomy |
get_diagnostics |
Live API reachability + version + mirror/cache/runtime metrics |
search_score_sets is the router's pinned entry point. Leaf names are unprefixed per
Tool-Naming Standard v1;
behind genefoundry-router they surface as mavedb_<tool> — e.g. mavedb_search_score_sets.
The server also registers the mavedb:// resource family (capabilities, tools, usage,
reference, research-use, citation) and a response_mode token-cost lever on every tool; see
docs/architecture.md.
Data & provenance
Upstream is the public MaveDB REST API
(https://api.mavedb.org/api/v1) — read-only, no credentials, no API key. The router never
forwards a caller's token upstream.
Refresh model: mirror-primary, live-backup. A local SQLite mirror is built from the CC0
MaveDB Zenodo bulk dump (concept DOI
10.5281/zenodo.11201736, always resolving to the newest version); a mirror-miss — for example
a record newer than the snapshot — falls back transparently to the live API. Each response
stamps _meta.data_source (mirror | live | mixed) and mirror_as_of. Full mechanics,
including the lazily-backfilled VRS/ClinGen layer: docs/data.md.
Data licence: per score set. MaveDB has no blanket data licence — each dataset carries its
own (CC0 1.0, CC BY 4.0, or CC BY-SA 4.0). Honour each record's license.shortName.
Citation. Cite the platform, and alongside it the specific score-set URN, its licence, and its primary publication:
Esposito D, Weile J, Shendure J, et al. MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect. Genome Biology. 2019;20(1):223. doi:10.1186/s13059-019-1845-6
MaveDB functional scores are experimental measurements, not clinical variant
classifications; a calibrated class such as abnormal/PS3 is assay evidence, not a
pathogenicity call.
Documentation
- Architecture — the MaveDB data model, the calibration layer, the response contract, and the
mavedb://resources. - Configuration — every
MAVEDB_LINK_*variable, the transport modes, and the Host/Origin request guard. - Data & the local mirror — the Zenodo dump, build/refresh commands, and the lazy mapped-variant cache.
- Deployment — the container stacks, the data-init container, bundle pinning, and the reverse proxy.
- Design spec · implementation plan.
- AGENTS.md — engineering conventions: the two-plane boundary, tool naming, and the mirror invariant.
Contributing
See AGENTS.md for engineering conventions and the repository layout.
make ci-local is the definition-of-done gate: format, lint, the line budget, the README
standard, mypy strict, and the tests.
License
MIT © Bernt Popp — this repository's code. Note the three layers: the MaveDB
platform code is AGPL-3.0, and each MaveDB dataset carries its own licence (CC0 1.0 /
CC BY 4.0 / CC BY-SA 4.0) — honour license.shortName on every record you use.
Установка Mavedb Link
У этого сервера нет опубликованного пакета — он собирается из исходников. Открой репозиторий и следуй инструкции в README.
▸ github.com/berntpopp/mavedb-linkFAQ
Mavedb Link MCP бесплатный?
Да, Mavedb Link MCP бесплатный — установка в пару кликов через Unyly без оплаты.
Нужен ли API-ключ для Mavedb Link?
Нет, Mavedb Link работает без API-ключей и переменных окружения.
Mavedb Link — hosted или self-hosted?
Self-hosted: сервер запускается локально на твоей машине командой из раздела установки.
Как установить Mavedb Link в Claude Desktop, Claude Code или Cursor?
Открой Mavedb Link на unyly.org, выбери вкладку своего клиента (Claude Desktop, Claude Code, Cursor) и нажми Install — конфиг сгенерируется автоматически, без правки JSON.
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