Transform complex genetic variations into actionable clinical insights with advanced machine learning. Analyze pathogenic variants, population frequencies, and pharmacogenomic markers through our unified AI platform.
Experience our AI-powered variant interpretation engine. Search any variant using HGVS notation, gene symbols, or rsIDs.
Illustrative examples of AI-assisted genomics workflows. Generic descriptive use; unaffiliated. Not for clinical/diagnostic use.
Illustrates ensemble-style scoring using public variant resources (e.g., ClinVar, COSMIC, gnomAD) to show how evidence can be combined for research/education. No affiliation implied.
Example allele-frequency lookups across sample populations to explain ancestry-aware summaries and founder-variant concepts.
Shows CPIC-style guideline lookups for educational purposes only. Not medical advice; no dosing recommendations. Names belong to their respective owners; no affiliation implied.
Illustrates how a FHIR-style API could exchange structured genetics data (VCF/HGVS) in principle. Demo only; no PHI collected or stored.
Accelerate rare disease diagnosis and cancer genomics interpretation
Identify therapeutic targets and predict drug response biomarkers
Streamline variant annotation and functional impact prediction
Conduct large-scale GWAS and epidemiological research
AlleleAI.com — The perfect domain for your genomics AI platform. Combining "Allele" (genetic variants) with "AI" instantly communicates cutting-edge genomic intelligence.