AI can organise and explain the evidence. It does not create the evidence.
Depth without discipline is just more numbers. These are the standards that make an integrated report trustworthy rather than merely impressive.
Laboratory and assay
Laboratory methods, quality checks and collection arrangements must be clear before measurements are reported. Provider details and any certifications will be confirmed before the programme opens.
- Document the method used for each measurement
- Record laboratory provenance and quality information
- Confirm provider and collection arrangements before purchase
- Direct medical questions to the client's clinician
Interpretation sources
Genomic interpretation is intended to draw on published evidence, with sources and versions documented. Medical records supply context; they are not independently interpreted as clinical care.
- Clinical variant and population frequency databases
- Published association and polygenic score catalogues
- Pharmacogenomic guideline resources
- Version stamped on every interpretation
The longevity signature
The 183-variant signature is read from the same 30× whole-genome sequence, not a separate assay. Its associations should be presented with evidence strength, effect size and limitations.
- Study-level traceability per variant
- Effect size published with the finding
- Four confidence tiers, reviewed on new evidence
- No over-claiming from small effects
Software and AI
The intended role of software is to organise and explain supported genomic and methylation information, not invent values or determine the medical significance of records.
- Grounded generation — no invented values
- Deterministic calculation of all reported figures
- Version the evidence used for explanations
- State uncertainty and limitations clearly
Medical boundary
Aevum organises medical results and history in the record but does not independently interpret them as care. Clinical decisions and follow-up belong with a qualified professional.
- Medical results recorded for context
- No diagnosis or treatment recommendation
- A report to bring to your own clinician
- Clinical follow-up remains with the care team
These describe the standards Aevum builds to. Aevum does not claim certifications, regulatory approvals, contracted clinical partners or advisory appointments that have not been formally confirmed.
What an Aevum report cannot do
Stating this plainly is part of the product, not a footnote to it.