Exon Research
Official@exon-research
Building local-first AI co-scientist for genomic research
Agent Skills by Exon Research
Showing 19 vetted skills indexed across 1 GitHub repositories.
genomi
Analyze local genome data with natural language queries for genetic insights.
journal
Manage investigation memory by linking Genomi evidence and research findings.
pharmacogenomics
Analyzes drug-response and pharmacogenomic questions using public PGx evidence and local genotype data.
clinvar
Build candidate landscapes and inventories from exact ClinVar variant matches.
prs
Apply published polygenic scores to personal DNA and calculate raw weighted scores.
journal-source-research
Review academic journal evidence and record findings into Genomi context.
genomi-gnomad
Fetch population allele frequencies for a specified variant from gnomAD.
functional-genomics
Retrieve and analyze perturbation evidence from BioGRID ORCS and DepMap.
analytical-grounding
Retrieve pathway members, cell-type markers, and genomic interval overlaps from biological databases.
genomi-decode
Assembles a comprehensive Genomi Dashboard.html from active genome data and Genomi capabilities.
variant-evidence
Analyze genetic variants using Active Genome Index and public genetics databases.
ancestry
Project genome data onto 1000 Genomes reference panels for ancestry analysis.
genomic-inquiry
Analyze DNA queries with natural language processing for genetic variant insights.
gwas-catalog
Compare candidate rsIDs and genes against GWAS Catalog phenotype associations.
rare-disease-cancer
Analyze public genetic data and genome evidence for rare disease and hereditary cancer risk.
active-genome-index
Digitizes and manages private genome data into a searchable Active Genome Index.
nutrigenomics
Analyze genetic variants for nutrient metabolism, food tolerance, and taste perception insights.
sequence
Translate DNA sequences, detect ORFs, and check primers locally.
drug-targets
Prioritize drug-targets using causal evidence from public records and Open Targets.
Frequently Asked Questions About Exon Research
FAQPage SchemaWhat specific genomic tasks can be performed using Exon Research?▼
Exon Research enables local analysis of DNA sequences, including variant interpretation, pharmacogenomic drug-response assessment, and rare disease risk evaluation. Users can perform ancestry projections, calculate polygenic risk scores, and cross-reference genetic variants against public databases like ClinVar, gnomAD, and the GWAS Catalog for comprehensive phenotypic insights.
Who is the target persona for these genomic research capabilities?▼
The target personas include bioinformaticians, genetic researchers, and clinical scientists requiring local-first processing of private genome data. These capabilities are designed for professionals managing large-scale variant inventories, performing functional genomics perturbation analysis, or investigating hereditary cancer risks through evidence-based, private computational research environments.
What are the primary dependencies for running these genomic analysis functions?▼
Execution requires a digitized Active Genome Index derived from private DNA data. The system relies on connectivity to public biological repositories, including BioGRID, DepMap, Open Targets, and the GWAS Catalog, to ground local sequence analysis in established scientific evidence and population-level allele frequency data.