openpgx
OfficialRelated Servers
Alternatives to openpgx
No user-submitted related servers found.
Related Servers
- AlicenseCqualityFmaintenanceProvides AI-powered access to major biological databases for GWAS and bioinformatics research. Enables natural language queries for protein, gene, variant, pathway, and drug discovery analysis.441MIT
- AlicenseNot gradedqualityDmaintenanceA local-first MCP server that annotates whole-genome VCF files and lets you query pharmacogenomics, disease risk, and carrier status through natural language.7MIT
- AlicenseNot gradedqualityDmaintenanceEnables real-time pharmacogenomics analysis, including variant clinical significance, drug-gene interactions, and dosing guidelines, by connecting to ClinVar, PharmGKB, gnomAD, and other databases.1MIT
- AlicenseAqualityBmaintenanceEnables AI agents to retrieve cited pharmacogenomic and gene-variant information, including drug–gene guidance from CPIC/DPWG and rsID lookups, so responses can quote curated sources instead of relying on memory. A local package also lets users read raw DNA files on their own computer without sending the file data to the remote service.243 PyPIMIT
- AlicenseNot gradedqualityDmaintenanceEnables AI agents to query clinical genomics databases, retrieve supporting literature, analyze population genetics, and visualize biological pathways.18MIT
- AlicenseAqualityBmaintenanceUpload your raw DNA file from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, or any VCF -- and watch a team of AI agents fan out across 16+ public genomics databases, share discoveries with each other in real time, and produce a comprehensive health report. Everything runs on your machine. Nothing is uploaded anywhere.2416MIT
TDQS
Scored across 16 tools
Several tools have overlapping purposes, notably the multiple 'full' report tools (diagnostic_all, full_pgx_report, full_report, full_risk_report) and multiple upload-related tools (upload_genome, upload_genome_chunk, upload_genome_start, get_upload_command, load_profile). Descriptions help but an agent could select the wrong one.
Naming patterns are inconsistent: some use 'verb_noun' (check_medication, upload_genome), others use 'adjective_noun' (full_report, trait_report), and some are compound (get_upload_command, upload_genome_start). No coherent pattern across the set.
16 tools cover a complex domain (pharmacogenomics, disease risk, traits, upload workflows) without being excessive. Each tool has a distinct role, though a few could potentially be consolidated.
The tool set covers major workflows: genome upload, medication and risk checking, comprehensive reports, and trait discovery. Minor gaps exist (e.g., no update/delete for saved research), but core needs are met.