"Python context management and dependency solving in ComfyUI" matching MCP servers:

MyChart MCP Server

An MCP server for querying the KEGG bioinformatics database, providing tools, resource templates, and guided prompts for pathways, genes, compounds, and more.

An MCP server that grounds protein research in the UniProt SPARQL endpoint, providing tools for querying proteins, sequences, variants, diseases, and more via intent-named tools and raw SPARQL.

Grounds gene-nomenclature work in the HUGO Gene Nomenclature Committee (HGNC) dataset, enabling resolution of gene symbols and IDs to canonical HGNC identifiers, plus cross-references and batch operations.

An MCP server implementing the ROBINS-I V2 framework for risk-of-bias assessment in non-randomized studies, with deterministic algorithms and full provenance. It enables users to parse study documents, specify target trial results, answer signalling questions with evidence-bound quotes, and compute or override domain judgements.

TransBench is a translational research agent that takes free-text clinical observations, decomposes them into biological axes, generates falsifiable hypotheses grounded in PubMed evidence, and designs reproducible computational experiments with concrete datasets for Claude Science.

Enables Claude Desktop to query and analyze diabetes data from Omnipod 5 and Glooko through natural language, providing clinical audit and triage insights such as time in range, trends, and bolus analysis.

SuperGlookoQuery is a Claude Desktop extension (MCPB) that connects to Glooko diabetes device data and exposes it as clinical analysis tools (time in range, GMI, trends, enriched bolus/basal analysis, charting), for any pump/CGM combination Glooko supports rather than one fixed device. It's a fork of Richard Hall's podquery-mcp, reworked to discover each account's own data shape rather than assumi

Monitors PubMed and medRxiv for configurable research topics, summarizes papers using a local LLM, and stores deduplicated results in a local database.

Taiwan's first public Model Context Protocol server for National Health Insurance data — rejection codes, ICD-10 mappings, audit indicators, semantic wiki search. Powered by OPDSTAR.

A Model Context Protocol (MCP) server for interacting with Gen3 data commons, with GraphQL query validation to reduce hallucinations.

Renders interactive 2D molecular structure diagrams from SMILES notation and computes molecular properties like molecular weight, LogP, and TPSA, directly in the chat.

Search 200M+ patents and scientific literature in natural language using PatSnap's global R&D intelligence database.

Enables AI assistants to answer healthcare REIT portfolio questions with deterministic, provable answers grounded in Omega Healthcare 10-K filings and CMS nursing home data, including status, caveats, and provenance.

A Claude Code extension that embeds a senior athenahealth integration engineer in your development workflow, proactively catching data loss bugs and guiding safe DataView queries and API integrations.

MCP server that provides tools for querying the Human Phenotype Ontology (HPO) including term lookup, hierarchy exploration, cross-ontology mappings, and gene-phenotype-disease associations, all grounded in a local SQLite database for fast offline lookups.

Provides phenotype-aware cardiovascular triage tools including FHIR R5 case retrieval, missing-data analysis, ECGFounder-backed ECG interpretation, risk summarization, and structured SBAR handoff in multiple languages.

Enables LLM agents to search biomedical literature, retrieve article details, find related papers, manage caching, and download open-access full texts through MCP with structured, agent-friendly responses.

Identifies plants from photos and determines whether a species is native, introduced, or invasive in a given country, drawing on GBIF, GRIIS, and GISD data, and also provides management recommendations and country alien-species lists.

Enables editing and querying of Gene Ontology Causal Activity Models (GO-CAMs) through the Barista API. Supports model creation, individual and fact management, evidence addition, and causal pathway construction for biological knowledge representation.