How it works

One genome. Four parts. A record that grows with you.

Your genome and methylation measurement form the starting point; medical records and wearable data keep the picture connected over time.

01
Onboarding and history
Share relevant history and tell us whether you already have compatible whole-genome data. These details are kept as context, not independently interpreted as medical care.
At home
02
Sample collection
Samples for 30× whole-genome sequencing, DNA-methylation age and a comprehensive blood biomarker panel are planned. Collection options and panel details will be confirmed before purchase.
Arranged individually
03
Genome and methylation
Your genome is sequenced at 30× depth; the 183-variant longevity signature is read from it. DNA-methylation age is measured separately as a repeatable baseline.
Two measurements
04
Bring your record together
The blood panel and any additional results, history and documents you share sit beside wearable and lifestyle data. The record organises these inputs without independently interpreting medical data as care.
Medical + everyday data
05
Your report
A plain-language view of genomic and methylation findings, with medical records and wearable trends alongside — ready to share with your doctor.
Delivered digitally

Your data

Measured once, kept in context

Genomic data is among the most sensitive personal data there is. These are the privacy principles guiding the programme.

The intended use is to produce and update your report, with any other use described separately.

The programme is being designed around specific consent for any optional secondary use.

Export, correction and deletion processes will be detailed in a formal notice before data collection opens.