"Automating Browser Operations with Scripting or Tools" matching MCP servers:

Scholarly integrity and papers — citation checks, literature/PubMed search, academic experts, PDF tables (6 MCP tools).

Enables clinical question answering via OpenEvidence with citation verification, including tools to ask questions, retrieve results, and follow up, plus an integrated skill to check citations against primary sources.

Provides in-process RDKit cheminformatics operations — descriptors, fingerprints, similarity and substructure search, reaction enumeration, standardization, and 3D conformer generation — for AI agents.

US federal money and filings — grants, contracts, SBIR/STTR topics, SEC financials, clinical trials (5 MCP tools).

Enables MCP-capable AI clients to characterize proteins end to end: PDB/mmCIF validation, sequence extraction and typing, pLDDT confidence summaries, metal-site geometry with bidentate chelate detection, GROMACS trajectory metrics and plots, and live UniProt, AlphaFold DB, and RCSB lookups. Also ships a point-and-click Protein Lab web UI (and a persistent run registry) so students and wet-lab biologists can get the same results without any client setup.

Enables LLM agents to query de-identified FHIR-shaped hospital data through audited, read-only tools for patients, encounters, conditions, observations, medications, and interaction checks, while any medication write stays a draft that a clinician must confirm out-of-band.

Provides FHIR resource validation, synthetic test fixture generation, and HIPAA-safe logging review as MCP tools for AI agents.

Provides comprehensive access to the UCSC Genome Browser API, enabling queries of genomic data, DNA sequences, gene annotations, variants, and metadata across multiple species and assemblies.

Enables AI agents to query free biomedical and pharmaceutical APIs for clinical trials, drug data, molecular structures, adverse events, and research literature.

Enables deep probabilistic analysis of single-cell omics data using scvi-tools through natural language. Supports SCVI for scRNA-seq analysis, SCANVI for cell type annotation, TOTALVI for multi-modal RNA/protein data, and PEAKVI for scATAC-seq analysis.

A specialized MCP server for Metal-Organic Framework research that provides tools for database searching, structural optimization, and energy calculations via ASE. It enables scientific workflows by allowing users to interact with MOF data and perform chemical simulations through a standard SSE interface.

Enables querying UCSC Genome Browser assemblies, annotation tracks, track data over genomic intervals, and raw DNA sequences across ~250 species without authentication.

Provides oncology data (research, news, FDA approvals, clinical trials) and IBM MAMMAL biomedical predictions (PPI, DTI, ClinTox) as MCP tools. Allows AI agents to query cancer datasets and run predictions through a remote MCP server.

Enables AI agents to read and analyze Dexcom CGM data through tools for current glucose, recent historical readings, and glucose statistics such as time in range.

Exposes four CMS public datasets as callable tools in Claude conversations, enabling natural-language real-world evidence analytics without SQL expertise.

Enables interaction with the CEDAR (Center for Expanded Data Annotation and Retrieval) metadata repository to fetch templates and retrieve template instances. Supports querying structured metadata and biomedical data annotations through the CEDAR platform.

Enables searching and fetching articles from PubMed, a database of biomedical literature.

Enables querying FDA drug label information including adverse reactions, warnings, and indications via natural language.

Provides programmatic access to ClinicalTrials.gov API with 18 specialized tools for searching, analyzing, and retrieving detailed information about 400,000+ clinical trials worldwide, including filtering by condition, location, phase, sponsor, eligibility criteria, and outcomes.

Provides access to an AI medical chatbot API for healthcare assistance, enabling natural language interactions such as neurosurgery queries.

Enables searching cryo-EM density maps in EMDB and raw datasets in EMPIAR, with filtering by resolution, keyword, and cross-referencing between the two databases.

An MCP server for clinical workflows with tools for patient lookup, appointment booking, prescriptions, drug interactions, symptom triage, lab results, insurance eligibility, and telehealth, enforcing role-based access control and audit logging.

Search Vascue's public healthcare-operations documentation: AI front desk for clinics, provider-side insurance claims automation, Cliniko integration, security. Public content only.

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.

Enables language models to search biomedical literature, fetch sequences, and follow links across Entrez databases through eleven read-only tools wrapping the nine NCBI Entrez E-utilities. It handles URL building, pacing, redirects, response caps, and API-key redaction so queries can be answered without a browser or scraping.

Exposes 24 evidence-grounded medical skills as JSON-RPC tools over stdio, letting agents run deterministic clinical calculators, PHI de-identification, negation-preserving multilingual parsing, and drug interaction checks locally with no token cost. It also enforces provenance and safety gates so high-risk dosing or prescribing decisions require documented clinical records rather than model inference.

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.

Enables scoring the WHO-5 Well-Being Index from five answers, returning a 0–100 score and a low, reduced, or normal band without providing a diagnosis.

Enables natural language querying of brain volumes (NIfTI) with a fixed set of tools, returning visualizations and reproducible nilearn code.

MCP server exposing REINVENT4 generative molecular-design operations as validated, LLM-callable tools for drug discovery, including sampling, transfer learning, reinforcement learning, and molecular analysis.

Enables AI agents to search a directory of Iranian doctors by full or partial name, city or province, and specialty, and returns the best match with alternatives plus clinic addresses, phones, weekly hours, and map links. It is read-only and requires no authentication, so it cannot book appointments or provide medical advice.

Enables read-only consultation of the latest published content on AI applied to medicine—articles, news, podcasts, lessons, events, conferences and repositories—through tools to list recent items, search by topic, and open item summaries with links.

Connects OpenEvidence to MCP clients for authenticated research queries using your browser session.

Enables a dental office's AI agent to verify benefits for a batch of up to 25 patients in a single MCP call, returning coverage percentages, frequency limits, waiting periods and deductible/annual-maximum remaining, each tied to a plan-clause citation. Exceptions such as identity mismatches or ambiguous cases are routed to a human review queue rather than guessed, with every call audit-logged.

Enables agents to interact with a clinic booking API, including listing specialties, doctors, and a patient's appointments, and booking or cancelling appointments when the active profile permits, while preserving the caller's authority and screening tool descriptions for safety.

Exposes a clinic's knowledge base and structured records to Claude Desktop as callable tools, with read tools grounded with citations and write tools gated behind approval.

Enables querying a synthetic patient dataset with tools to look up patients by ID, age, disease, name, and get statistics, connecting Claude Desktop to local data.

Enables AI-assisted molecular biology experiment design with tools for qPCR primer design, cloning strategy optimization, TaqMan probe design, and multiplex compatibility analysis.

Generates family pedigree tree diagrams as PNG or SVG images using standard genetic notation compliant with Bennett 2008/2022 NSGC guidelines. Supports comprehensive genealogical features including conditions, genetic testing results, twin relationships, carrier status, and adoption indicators.