Why Spoke exists
Built for the moment a pattern starts to make sense.
A result feels like you. An unexplained experience begins to make sense. A confusing mass of health information becomes more ordered. Spoke DNA is designed for that shift.
The customer journey
From recognition to agency.
- 01Recognition
Something here feels recognisably you.
- 02Understanding
The pattern becomes easier to make sense of.
- 03Prioritisation
You can see what deserves attention and what can wait.
- 04Agency
You leave with a practical next conversation or check.
A founder's note
Interpretation should reduce the burden of knowing.
“I started Spoke because I wanted the kind of careful interpretation I would want for my own health.”
My background is in genomics, cancer biology, drug discovery, and AI-enabled science. Spoke brings that evidence discipline to personal genomics without turning DNA into a diagnosis or a fixed blueprint. The aim is simpler: help someone recognise what may be relevant, see where to focus, and know what can safely remain in the background.
- PhD in Cancer Research, Imperial College London
- MSc in Immunology, London School of Hygiene & Tropical Medicine
- BA in Biological Sciences, University of Oxford
- Former senior scientist and Sable Bio co-founder
What useful feels like
Clearer, not busier.
A good report should not leave you with a longer health to-do list. It should create order.
- 01
Recognition
A finding confirms something you had noticed, or gives a familiar experience a more useful frame.
- 02
Direction
A confusing mass of health information becomes a shorter list of what may be worth checking and what can wait.
- 03
Trusted interpretation
Someone has helped you make sense of the evidence responsibly, including where it is limited or needs clinical confirmation.
The product
A report that tells you what matters first.
The Complete report is organised around priorities, evidence, and the next useful decision, not the number of traits a file can produce.
- What may be worth checking now
- What can wait or stay in the background
- What could be useful to discuss with a doctor
Start with fit
See whether your existing DNA file is suitable.
The check is free and private. You choose a report only after fit is confirmed.