Built on peer-reviewed science
Understand your genome.
Personalise your health.
Upload raw DNA data from 23andMe, AncestryDNA, or MyHeritage. Receive AI-powered insights into health risk, drug compatibility, ancestry, and rare conditions — reviewed against peer-reviewed evidence.
- 23andMe compatible
- AncestryDNA compatible
- MyHeritage compatible
A platform for everyone in genomics
Built for individuals, clinicians, and researchers.
For individuals
Upload your raw DNA file and receive personalised health, ancestry, and trait insights.
Explore features →For clinicians
Clinical decision support, pharmacogenomics, and patient genomic profile management.
For clinics →For researchers
Genomic AI tools for discovery, stratification, and biomarker analysis.
For researchers →What you can learn from your genome.
Health risk report
Predisposition scores for 50+ conditions, contextualised against population data.
Pharmacogenomics
How your genes affect medication response, with dosage and avoidance guidance.
Ancestry & traits
Ethnic breakdown, migration paths, and trait predictions.
Nutrition & fitness
Genome-informed diet, exercise, and supplement guidance.
Rare disease screening
Variant flags cross-referenced with curated rare disease databases.
AI genomics Q&A
Ask plain-English questions and get evidence-linked answers.
Not medical advice. AI-generated insights are educational only. Always verify with a qualified healthcare professional.
Ready to read your own genome?
Join the waitlist for early access to upload, analysis, and personalised reports.