exon-research/genomi

genomi

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

원문 언어: 영어

genomilab

Run or continue patient-authorized, genome-informed GenomiLab investigations in the current Claude, Codex, or other MCP agent task. Use when a patient asks to open the Research Desk, investigate a condition against their active genome, review an existing…

원문 언어: 영어

variant-evidence

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

원문 언어: 영어

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…

원문 언어: 영어

clinvar

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

원문 언어: 영어

genomi-decode

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 compose every capability's findings into a single artifact. This…

원문 언어: 영어

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.

원문 언어: 영어

rare-disease-cancer

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

원문 언어: 영어

ancestry

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

원문 언어: 영어

drug-targets

Causal drug-target and mechanism gene prioritization from public source records, drugs, drug classes, mechanisms, and candidate gene lists.

원문 언어: 영어

functional-genomics

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

원문 언어: 영어

genomic-inquiry

Default entry for natural-language DNA questions. The host agent resolves intent, reads focused skills, calls narrow evidence tools, and adapts after inspecting tool output.

원문 언어: 영어

genomi-gnomad

Fetch reusable public population allele frequencies from gnomAD for a specific variant. Use when the user asks about allele frequency, MAF, population stratification, gnomAD numbers, or rarity of a specific allele.

원문 언어: 영어

gwas-catalog

Compare candidate rsIDs against GWAS Catalog phenotype associations. Use association evidence with source and ancestry limitations.

원문 언어: 영어

journal

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

원문 언어: 영어

nutrigenomics

Curated single-marker evidence for declared nutrient-metabolism, food-tolerance, and taste-perception domains. Refuses diet prescriptions, supplement dosing, weight-loss prediction, methylation-cycle prescriptions, microbiome-mediated effects, and other…

원문 언어: 영어

journal-source-research

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

원문 언어: 영어

analytical-grounding

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

원문 언어: 영어

sequence

Deterministic sequence utilities for translation, ORFs, restriction sites, Kozak context, primer checks, and local FASTA record matching.

원문 언어: 영어

prs

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

원문 언어: 영어