We built the report we could not buy
Aevum was conceived in response to a market that often sells single biological signals as complete answers.
The tools to understand inherited longevity biology and current biological state now exist separately and affordably. Whole-genome sequencing at clinical depth has fallen to consumer prices. Methylation clocks are repeatable. Clinical biomarkers are routine.
What does not exist, outside programmes costing many thousands, is the work of reading genomic and methylation findings clearly while keeping blood results, history and wearable trends in one longitudinal record for a clinician to review.
That is what Aevum is building: 30× whole-genome sequencing with its 183-variant longevity signature, DNA-methylation age, a medical-data record and wearable context in one report. Medical results are recorded, not independently interpreted as care.
Our operating principle is simple: never claim more than the evidence supports, and never let caution flatten a finding that genuinely matters.
Honest before impressive
If the evidence is weak, the report says so — even where a bolder claim would sell better.
Connected before exhaustive
Genomic and methylation findings are easier to understand beside your dated records.
Longitudinal before one-off
The genome is measured once; the understanding is built continuously.
Supportive before autonomous
Medical assessment belongs with your clinician; the record never stands in for one.
Built on operations, not on a pitch
The programme is being designed around traceable measurements, clear interpretation boundaries and a record that can be updated.
Evidence-led interpretation
Genomic and methylation findings explained with uncertainty and limits stated plainly.
Measurement plan
Sequencing and methylation methods are being specified alongside collection arrangements.
A curated signature
A 183-variant longevity signature read from the whole-genome sequence and described with evidence strength.
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