One-off
Deep Analysis
€149once · yours to keep
- Everything you upload, read together
- Full findings with sources and evidence tiers
- Your first set of N-of-1 experiments
- Export anything, delete everything
N-of-1 health intelligence · private beta
You already own
this data.
Now read it.
Your genome sits in a file you opened once. A decade of your wearable history is trapped in an app. There's a scan disc in a drawer. N1Vector reads all three together — and keeps reading as the record grows.
Signals convergeOne trajectory
The corridor narrows as evidence accumulates
Nothing to buy.
Nothing to book.
No blood draw, no appointment, no device to wear. N1Vector works on the files you already have — which is why you can start this afternoon.
You already have it
Your genome
The raw file from 23andMe or Ancestry. Pharmacogenomics, carrier and trait calls, and polygenic scores — each with its evidence tier, ancestry applicability and limits stated plainly. Sensitive layers stay off until you switch them on.
You already have it
Your history
Years of sleep, heart rate, HRV, blood pressure, workouts, labs and body composition — exported from Apple Health or connected directly. Kept losslessly, so nothing is flattened into a daily grade.
You already have it
Your scans
The DICOM disc from the clinic. De-identified on arrival, then measured: hippocampal and ventricular volumes, white-matter changes — with normative context and scanner caveats attached, tracked from one scan to the next.
It isn't a report.
It's a loop.
A one-off analysis is read once and forgotten. The value is what happens in the fourth month — when something has moved and you find out why.
01
It reads everything
Genome, history and scans in one pass — not one app, device or specialty at a time.
02
It notices change
Longitudinal diffing surfaces what actually moved since last time, instead of restating the same findings forever.
03
It proposes a test
Genotype proposes; your data confirms. A variant becomes an N-of-1 experiment, not advice.
04
It says what to measure
Not more data — the one measurement that would most reduce the uncertainty about you.
Grounded, or silent.
The failure mode of AI health advice isn't too little data — it's confident nonsense. These constraints are enforced in the system.
It cites, or it says nothing
Retrieval over verified clinical guideline cards. No facts invented, none fine-tuned in.
Never a bare number
A polygenic score always ships with coverage, ancestry applicability and context. Low-coverage scores are suppressed outright.
Evidence tiers, always
Every genetic finding carries its evidence level, its actionability — and the words "not a diagnosis".
Caveats travel with results
Morphometry arrives with normative percentiles and scanner-protocol confounds attached.
Consent before computation
Sensitive layers are gated before anything is calculated, not merely hidden at display time.
It never pretends to be your doctor
N1Vector does not diagnose, does not treat, and will not tell you to change a medication. It prepares you for the people who do — with the questions worth asking and the evidence to ask them with. Clinical concerns are flagged for professional review, not resolved here.
Not a medical device · Not a diagnosisRead it once.
Or keep reading.
You bring the data, so there's no lab bill inside the price. Start with one deep analysis; subscribe only if you want it to keep watching.
Subscription
The Loop
€19per month · or €180 a year
- Everything in Deep Analysis, re-run as data arrives
- Continuous ingest from your wearables
- What changed since last time
- New experiments and next-best measurements
Who this is for.
It suits a particular kind of person, and genuinely doesn't suit others.
Built for you if
- You already have data — a genome file, years of wearable history, or scans
- You want to know how good your body can actually get
- You value evidence you can inspect over confident summaries
- You're willing to run an experiment on yourself and wait for the answer
Not the right fit if
- You want a diagnosis, or an answer today
- You want another step counter, meal logger or streak
- You expect genetics to predict your future with certainty
- You want medical treatment decided without a professional
Held properly.
Genome, scans and health records are special-category data under GDPR. We hold them as a custodian, not as an asset.
European by default
Stored and processed on EU infrastructure, under EU law, with a named controller.
Encrypted per person
Per-user keys, with the sensitive layers isolated rather than pooled.
Never sold, never trained on
No broker, no ad tech, no research resale. Your genome does not become anyone's model weights.
Leave whenever
Export everything, or delete everything, in one request — honoured in full.