yo-steven/genomi-exploration-20260613

genomi

Use this skill for genetics, genome source, variant, gene, phenotype, disease, screen, pharmacogenomics, and Genomi install/setup maintenance questions.

active-genome-index

Register, parse, and digitize private genome source files into a local Active Genome Index and supporting evidence stores. Use when the session explicitly supplies a VCF/gVCF, BAM, genome.computer .genome/1.0 bundle, 23andMe raw genotype export, AncestryDNA…

clinvar

Build and inspect ClinVar exact-match evidence and candidate inventories. Use for clinical labels, VUS/conflict, carrier context, and drug-response rows.

genomi-decode

Activate this skill for "/genomi decode", "decode my genome", "decode my DNA", "show me the dashboard", "the Genomi dashboard", "full report", "one-shot rundown", or any all-at-once request that asks Genomi to compose every capability's findings into a single…

pharmacogenomics

Answer drug-response, medication, PharmGKB-style, PGxDB, ATC, DrugBank, gene-drug, and variant-drug questions using public PGx evidence plus local sample genotype support when an Active Genome Index is selected.

rare-disease-cancer

Plan rare disease, hereditary disease, and cancer risk source investigation from public targets or selected active genome evidence.

variant-evidence

Answer specific rsID, allele, gene, region, genotype, and absence/callability questions using explicit session context or public evidence.