Retrieve pharmacogenomics data linking genetic variants to drug response. Explore how genetic variations affect drug efficacy and safety.
MIT
550,362 tools. Updated 2026-09-11 21:22
"Research on Patient-Disease-Gene-Drug Relationships and Pharmacogenomics Using Digital Imaging Data" matching MCP tools:
- Retrieve drug-gene interactions and pharmacogenomics data from PharmGKB by querying genes, drugs, or variants.MIT
- Run a comprehensive genomic report covering pharmacogenomics, disease risk for 19 conditions, and 30+ genetic traits with evidence, odds ratios, and citations.MIT
- Generate a complete genomic intelligence report combining medication pharmacogenomics, disease risk assessment, and trait analysis for personalized health insights.MIT
- Search NIH-funded research projects by topic, disease, investigator, or institution. Returns project details, award amounts, and PI names to track funding and identify researchers.MIT
- Search FDA adverse drug event reports by drug name, with optional MedDRA reaction filter, to retrieve seriousness flags, patient demographics, reactions, and drugs involved.MIT
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- Retrieve active medical problems for a patient using patient and clinic identifiers.MIT
- Resolve free-text disease names to GenCC catalog entries using title, MONDO, or OMIM ID. Returns ranked diseases with gene and submitter counts to inform gene-disease validity lookup.MIT
- Retrieve detailed gene-disease assertions: submitter classifications, inheritance modes, evidence links, PMIDs, consensus, and conflict analysis.MIT
- Rank diseases and genes by HPO phenotype similarity, retrieve entity records, and traverse gene-disease-phenotype associations from the Monarch Initiative biomedical knowledge graph.MIT
- Retrieve comprehensive biomedical data for articles, clinical trials, genes, drugs, diseases, and variants using unique identifiers. Standardized format supports detailed research and analysis across domains.MIT
- Retrieve all recorded patient allergies to identify substances to avoid and enable safe drug interaction checks.MIT
- Fetch all genes asserted for a disease, each with consensus classification and conflict flag. Query by MONDO/OMIM ID or disease title to get harmonized gene-disease validity data.MIT
- Profile top drug targets for common diseases by category, mapping each curated MONDO disease to its top Open Targets evidence-scored targets for a full landscape scan.Apache 2.0
- Execute pre-built queries on Alliance of Genome Resources data to retrieve gene orthologs, GO terms, disease associations, and other genomic information using parameterized templates.MIT
- Batch retrieve gene-disease validity assertions for up to 20 genes in a single request, returning consensus diseases and handling unresolved inputs gracefully.MIT
- Filter aggregated gene-disease validity assertions by classification, submitter, inheritance mode, gene, disease, or conflict status, with pagination. Retrieve harmonized GenCC data for targeted curation needs.MIT
- Retrieve a UniProt protein entry by accession and return its function, organism, disease associations, and cross-references.Apache 2.0
- Produce a one-call UniProt entry dossier for drug-discovery workflows, summarizing function, structural evidence, drug targets, disease links, variants, and annotations to guide deeper analysis.Apache 2.0
- Rank existing clinical-stage drugs as repurposing candidates for a given disease using Open Targets genetic evidence and clinical phase.Apache 2.0
- Search PubMed for peer-reviewed biomedical literature. Retrieve up to 10 papers per query on research, drug mechanisms, clinical outcomes, and disease studies.MIT