Research & Science · By exon-research

A skill your agent uses for genetics, genome source, variant, gene, phenotype, disease, screen, pharmacogenomics, and Genomi install/setup maintenance questions.

exon-research/genomi

Fetch reusable public population allele frequencies from gnomAD for a specific variant.

exon-research/genomi

Run or continue patient-authorized, genome-informed GenomiLab investigations in the current Claude, Codex, or other MCP agent task.

exon-research/genomi

Retrieve canonical pathway members, cell-type marker records, and genomic interval feature overlaps from declared analytical sources.

exon-research/genomi

Use local ancestry reference-panel tools for 1000 Genomes GRCh37/GRCh38 PCA projection, marker overlap QC, and qualitative reference-neighbor context.

exon-research/genomi

Build and inspect ClinVar exact-match evidence and candidate inventories.

exon-research/genomi

Register, parse, and digitize private genome source files into a local Active Genome Index and supporting evidence stores.

exon-research/genomi

Activate this skill for "/genomi decode", "decode my genome", "decode my DNA", "show me the dashboard", "the Genomi dashboard", "one-shot rundown", or any all-at-once request that asks Genomi to…

exon-research/genomi

Candidate gene evidence from perturbation, dependency, resistance, sensitivity, viability, or assay-context records.

exon-research/genomi

Default entry for natural-language DNA questions. An agent skill from exon-research/genomi.

exon-research/genomi

Compare candidate rsIDs against GWAS Catalog phenotype associations.

exon-research/genomi

Maintain agent-authored investigation memory over Genomi evidence links, reviewed source findings, decisions, contradictions, and unresolved questions.

exon-research/genomi

Journal sub-skill for focused public/source evidence review and reviewed finding write-back before interpretation or answer synthesis.

exon-research/genomi

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…

exon-research/genomi

Apply published polygenic scores from PGS Catalog to approved local personal DNA and return raw weighted score plus overlap QC.

exon-research/genomi

Plan rare disease, hereditary disease, cancer risk, carrier-relevance, and observed-condition source investigation from public targets or selected active genome evidence.

exon-research/genomi

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

exon-research/genomi