Example result · fictional profile
Demo modeMCM6 / LCT · rs4988235
RAW DNA FILE ANALYSIS / 100% LOCAL
Your variants, illuminated by selected scientific references.
Educational information · not a diagnosis.
Example result · fictional profile
Demo modeMCM6 / LCT · rs4988235
YOUR FILE, YOUR DEVICE
Compatible formats and services
Before uploading your file
After local processing, available variants are matched against selected scientific references to make their level of evidence, context, and limitations easier to explore.
KEY FEATURES
One experience to read your signals with method: every step adds a landmark, context, and a clearly visible limit.
01 / LOCAL
Your DNA file is read in the browser for standard analysis, without leaving your device.
02 / PRIORITIES
Find the reading points to explore first before moving through every detail.
03 / AREAS
Nutrition, sleep, movement, and other areas stay separate to keep the reading nuanced.
04 / CONTEXT
A personalization questionnaire connects signals with your goals and preferences.
05 / OPTIONAL AI
A structured summary can be generated from derived signals, only after your consent.
06 / REPORT
Keep a complete reading as a PDF and restore your purchase with the exact file.
KNOWLEDGE, NOT CERTAINTY
Every layer of the product distinguishes what is observed, what the literature supports, and what still needs careful interpretation.
The raw file is read on this device.
Variants are arranged into reading themes.
Sources and limits remain visible throughout.
SIGNAL / PLAIN LANGUAGE
THE DEMO IS PART OF THE PRODUCT
Start with a complete fictional dossier. See the reading architecture, the available previews, and what intentionally stays protected.
WHAT WE ORGANIZE
Colours are visual wayfinding. Topics stay separate so a raw file is never turned into an oversimplified narrative.
Lactose, gluten, caffeine, alcohol, vitamins, iron, omega-3, weight
Endurance vs. strength, tendons, inflammation, recovery
Chronotype, stress, dopamine, serotonin
Drug metabolism, coagulation, indicative markers
Lactose, gluten, histamine, fructose, microbiome, and gut comfort
Sun and photoaging, perspiration, tastes and odors
COMPLETE REPORT / ONE-TIME PURCHASE
The complete report extends exploration with more results, their scientific context, and a structured summary. It does not replace medical advice.
GENOSTRIDE / COMPLETE READING
Three offers, no subscription
No subscription · no account · one-time payment
The demo first shows the frame and the available previews.
CHOOSE YOUR ACCESS
Compare the contents, price, and data processing before importing your file. No subscription or account is required.
0 €
Import your DNA file and explore two variants per area for free, directly in your browser.
To check your file's compatibility and discover the interpretation framework before any purchase.
The preview, your DNA file, rsIDs, and genotypes stay on your device. No payment, account, or transfer is required.
Import my file for free€39
All available interpretations for this DNA file are processed 100% locally on this device, with no subscription.
To explore all results, their sources, and the PDF report, without the AI Plan.
Your DNA file, rsIDs, and genotypes stay on this device. The AI Plan is not included.
Choose and import my file€49
The complete analysis and Personalized Plan in a single purchase, instead of €58 separately.
To get the entire GENOSTRIDE experience immediately and save €9.
The Complete Analysis remains 100% local. The AI Plan is optional and requires your consent to send pseudonymized derived signals.
Choose and import my file+€19
An add-on to a previously purchased full analysis.
A structured plan, with optional AI assistance based on pseudonymized derived signals.
To turn a completed analysis already active into an actionable, structured plan.
Available after the Complete Analysis. With your consent, AI receives pseudonymized derived signals—never your DNA file, rsIDs, genotypes, or gene names.
Choose and import my file
HOW IT WORKS
Your file, made easier to read with scientific context.
GENOSTRIDE is a reading and visualization tool for an existing DNA file: it does not sequence your DNA or create a new test. It organizes the detected variants, places them alongside selected scientific references, and makes the evidence level, context, and limits of each reading visible.
Scientific knowledge and references evolve. They are provided to inform your reading, not to claim completeness or predict your health, future, or any individual outcome.