Wearable health data sync
Import activity, heart rate, sleep, and other vitals from Apple Health, Huawei Health, Xiaomi Health, and more. Your genomic profile gets richer with every data point.
INTERPRÉTATION GÉNOMIQUE
Vos données génomiques, prêtes à interpréter
Importez vos fichiers bruts génomiques existants et recevez des orientations continues sur votre appareil.
Gratuit pendant la bêta
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Quelle est votre situation ?
Comparaison
Fern Gene vs. services traditionnels
Sequencing labs deliver a report. We deliver continuous interpretation.
Sequencing labs
Fern Gene
What you get
One-time report snapshot
Continuously updated interpretation
Drug guidance (PharmGKB/CPIC)
Limited or not included
150+ rules, auto-updated
Carrier screening
May include, but static
Dynamic + partner joint screening
Family analysis
Not available
Trio analysis, partner review, cross-generational tracking
Wearable integration
Not available
Apple Health, Huawei, Xiaomi, Samsung, Google Fit
Report updates
Never updated after delivery
Rule engine refreshes as research evolves
Data location
Their cloud servers
Your device only
Re-interpretation cost
Pay again for new analysis
Free as rules evolve
What you get
Sequencing labs: One-time report snapshot
Fern Gene: Continuously updated interpretation
Drug guidance (PharmGKB/CPIC)
Sequencing labs: Limited or not included
Fern Gene: 150+ rules, auto-updated
Carrier screening
Sequencing labs: May include, but static
Fern Gene: Dynamic + partner joint screening
Family analysis
Sequencing labs: Not available
Fern Gene: Trio analysis, partner review, cross-generational tracking
Wearable integration
Sequencing labs: Not available
Fern Gene: Apple Health, Huawei, Xiaomi, Samsung, Google Fit
Report updates
Sequencing labs: Never updated after delivery
Fern Gene: Rule engine refreshes as research evolves
Data location
Sequencing labs: Their cloud servers
Fern Gene: Your device only
Re-interpretation cost
Sequencing labs: Pay again for new analysis
Fern Gene: Free as rules evolve
Fondement scientifique
Interprétation fondée sur les preuves
Domaines d'interprétation
+
Règles de production
+
Points de contenu
+
Sources de preuves
- •ClinGen, ClinVar, and GeneReviews — hereditary disease and clinical boundaries
- •PharmGKB and CPIC — pharmacogenomics: medication response, dosage, and metabolism
- •GWAS Catalog, PubMed, and Europe PMC — risk, nutrition, lifestyle, and lab follow-up
- •SNPedia — structured variant annotations, locally mirrored and checked
- •Professional guidelines for carrier screening, cancer predisposition, and pharmacogenomics (ACMG, NCCN)
Accueil Radar
Détail Salle des Preuves
Écran avis du partenaire
Intégration santé
Connecté à votre écosystème de santé
Les données génomiques sont plus utiles lorsqu'elles sont liées à votre historique médical
Apple HealthApple WatchHuawei HealthXiaomi HealthSamsung HealthGoogle Fit
Checkup report upload
Upload your annual physical exam reports — blood work, liver function, lipid panels — and see them interpreted alongside your genomic risk baselines.
AI health assistant
Ask questions about your genomic results, medication interactions, or follow-up priorities. On-device AI assistant gives answers grounded in your data and checked evidence sources.
Nos limites
Ce que nous ne faisons PAS
Your data is never used for insurance underwriting
Fern Gene does not feed into insurance risk assessment. No underwriter, actuary, or claims adjuster receives genomic data from this platform. This is a firm boundary, not a policy subject to change.
Advisors only see what you choose to share
Insurance advisors act as family account managers. They see status and next-step recommendations, not specific genotypes or variant calls. Access to detailed results requires your explicit consent for each category.
Your files never leave your device
Import, analysis, and storage happen entirely on your device. No raw VCF, gVCF, BAM, or CRAM file is uploaded to any cloud server. Online services use only minimal status metadata — never raw genomic data. This architecture naturally satisfies GDPR (no cross-border data transfer), HIPAA (no PHI transmission), and PDPA (no data collection requiring consent) without requiring data-processing agreements.
Statut de la plateforme
Disponibilité actuelle
Backed by 400+ medical institution partnerships and international pharmaceutical collaborations.
iPhone
Primary platform. Full consumer experience — onboarding, import, results, family account, partner review, and policy screens.
Android
Verified on real devices. Onboarding, import, results, Vault, partner review, and policy screens all confirmed working.
macOS
Desktop companion. Better suited for heavier BAM and CRAM files. Uses the same local analysis engine.
Windows
Planned. Same desktop-companion role as macOS for heavier workflows.
Témoignages
WeGene file plus 23andMe file, 15 minutes. The carrier screening flagged both of us as SMA carriers. Our OB-GYN said without this we would have found out after.
M., Shenzhen
Expectant parent
My mother had breast cancer at 42. The BRCA screening gave me a specific answer instead of generic anxiety. Turns out I don't carry the variant. That clarity is worth everything.
S., Hangzhou
Family history
My father takes seven medications. The multi-drug interaction check found a major interaction between his warfarin and the new antibiotic. His doctor adjusted the dose before discharge.
T., Beijing
Caregiver
Questions fréquentes
Is this another genetic testing service?
No. Fern Gene does not run sequencing. You bring raw files you already own, or get them from a lab first. The platform handles interpretation, ongoing updates, and family-level operations after import.
Can insurance companies access my data?
No. This platform is never used for underwriting, pricing, or claims. That is a structural red line, not a privacy policy. Raw files stay on your device and advisors never see detailed genetic results by default.
What do I actually see after importing?
You see prioritized guidance — medication responses, risk signals, carrier status, and lab follow-up items. 17 areas already have live results. Detail views include evidence sources and next steps. Everything updates as the rule engine evolves.
Can same-sex couples or non-traditional families use the family account?
Yes. Family accounts do not require marriage. Same-sex couples planning through IVF, donor egg/sperm, or surrogacy can use joint carrier screening the same way. HRT pharmacogenomics for transgender partners is already covered. Chosen families and co-parents can also share accounts.
How much does Fern Gene cost?
Importing and basic interpretation is free. Premium features like family accounts, partner review, and AI health assistant are available through subscription. During early access, all features are included at no charge.
Is Fern Gene compliant with GDPR, HIPAA, and PDPA?
Yes. Because all analysis runs locally on your device and raw files never leave it, Fern Gene does not transmit protected health information across borders. This architecture naturally satisfies GDPR data-minimisation requirements, HIPAA safeguards for PHI, and Singapore's PDPA consent framework — without requiring complex data-processing agreements.