Lisgen(01) The measurement(02) What you get(03) The evidence(05) The protocol(06) The boundary

Your body, measured to the DNA level.

Lisgen tells you what changed, what is coming, and what actually moves it — calibrated to you rather than to a population average. Your lab calls a 3 kg drop in strength normal variation. For you it may be the first real signal.

01

A reference range answers the wrong question

It tells you how you compare to strangers. What matters is whether your own number moved.

Standard panel · Population reference

Your grip strength is within normal range.

A published minimal detectable change of 5.0 kg is an average across strangers. It cannot tell you whether a 2.7 kg drop is noise for you or the third step of a real decline, because it was never about you.

Lisgen · Your own threshold

You dropped 2.7 kg. That is beyond your threshold of 2.36.

Third consecutive decline, slope −0.24 kg per month, 90% interval excluding zero. Your threshold came from your own measurement scatter under a stated protocol — and we widen it when the protocol slips.

How the thresholds are set

02

What you get6

Each measured on you rather than inferred from a cohort you may not belong to — including the things we decline to measure.
Mechanism611,131

Which pathways are yours

Tissue-resolved regulatory mapping across your genome. Not a risk percentile — the machinery itself, and therefore what to watch and where.

Organs11

What is aging fastest

Organ-specific aging ranked against your own other organs. Accelerated heart aging carries a 250% higher heart-failure risk.

Response4–8 wk

Whether it is working

Pace of aging responds in weeks, not years. Across 51 harmonised intervention studies it ranked among the most responsive of 16 clocks — though clocks disagree on some interventions, and we say which.

Experimentn-of-1

What works for you

Real experiments on your own body. Food, sleep, training, medication — your effect with your uncertainty, not a population average.

Drugs12 genes

How you metabolise

Pharmacogenomic phenotype from your sequence, the one place genotype legitimately changes a prescribing decision. Never a dose, never a drug name.

Boundaries57

What we refuse to claim

Every refusal carries the study that forbids it. Published as a machine-readable resource, so the limits are checkable rather than asserted.

03

Every competitor compares you to strangers. Lisgen compares you to you.

And gets sharper with every measurement you take. A competitor launching in eighteen months starts at zero on every user.

Body

Strength, fitness, metabolism, appearance.

Ten instruments with a published minimal detectable change, each tracked against your own scatter. Resistance training carries an all-cause hazard ratio of 0.87; protein at 1.2–1.5 g/kg/d with training adds 0.39 kg lean per 0.1 g increment.

Mind

Where a personal baseline matters most.

There is no meaningful population range for mood. Sleep regularity, activity and mobility shift one to four weeks before a downturn becomes obvious. We detect the change against your own pattern and name which of your factors drives it. We never hand you a diagnosis.

04

What the evidence supports

Ranked by effect on outcomes that matter, not on biomarkers that move easily.

05

A threshold is only as good as the protocol

Published minimal detectable changes are earned under supervision. We widen yours when the conditions do not match.

Device · Same task, same night

Your wearable decides more of the error than your protocol.

On nocturnal resting heart rate against an ECG criterion: Oura Gen 4 at 1.94% mean error, WHOOP at 8.17%, Polar Grit X at 16.32%. A device whose own error exceeds the change you are looking for cannot carry the claim, so we refuse it rather than quietly averaging it in.

Labs · Biological variation

Most analytes cannot be read against a population range at all.

Every analyte except serum water shows marked individuality. Where the index of individuality is low, a reference range carries almost no information about you — only your own history interprets the result. We use the published within-subject variation to compute what change is real for you.

06

One thing we will not sell you

The boundary is the product. Every refusal carries the study that forbids the claim.

Refuted · GENEROOS randomised trial

Your DNA does not predict how you respond to a diet.

A randomised trial took people at the extremes of genetic predisposition through a six-month dietary intervention and found nothing — P = 0.94. Every company selling genotype-based meal plans is selling a result that failed to replicate.

Supported · What sequence is for

Mechanism, and what to measure.

What your DNA does is tell us which mechanisms are yours and what to measure. Then we measure it. That is a better product, and it is still standing when someone checks.

The pre-registration