clinvar-database

SKILLWorkflowcommunauté
v0.0.0x-cmdApache-2.0Mis à jour il y a 1 moisSource →

Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.

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1Clients
1Formats
il y a 1 moisDernière mise à jour
Skill
Auteurx-cmd
Version0.0.0
LicenceApache-2.0
CatégorieWorkflow
Formatsskill.md
PromptNon publié
Compatibilité
Claude✓ Pris en charge
Cursor
Copilot
ChatGPT
Gemini
À propos

Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.

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