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DNA-Powered Health Intelligence

Know Your Exact Biology.
Build Protocols From Your DNA.

Your DNA contains the blueprint for how your body handles inflammation, repair, energy, and aging. GeneOS reads that blueprint — and turns it into a precise, personalized protocol. For you. For your patients.

🧬 Get Your DNA Kit ▶ See What You’ll Get

One-time payment · Lifetime access · No subscription ever · Encrypted results delivered by our certified lab

8.3M+ Verified Research Data Points
8,000+ Peer-Reviewed Studies in AI Training
18,000+ Gene Variants Mapped Per Profile
194 Peptide Compounds in the Matrix
Loading… DNA Kits Processed
Live
<48hr From Sample to Blueprint
🧬 For Individuals

Your DNA Contains a
Precision Blueprint
You’ve Never Seen.

GeneOS analyzes 18,000+ of your gene variants — how you metabolize nutrients, handle inflammation, respond to peptides, manage stress, and age. Then Hypatia AI builds you a personalized 12-week protocol. One test. For life.

🧬Genetic blueprint in <48 hours. 18,000+ variants mapped by pathway — methylation, inflammation, detox, hormones, metabolism, recovery.
🧠Your bio-age score. See whether your biological age is ahead or behind your chronological age — and which variants are driving the gap.
📋12-week personalized protocol. Supplements, peptides, nutrition, and timing — designed for your allelic profile. Not a template. Your biology.
♾️Lifetime access to your health console. No monthly fee. No subscription. Ever. GeneOS grows with your data forever.
🔬A structured laboratory workflow. Your sample and results move through a tokenized GeneOS workflow into your private health console, with encrypted delivery and no data-broker resale.
DNA Kit + Lifetime Access
One-time purchase. Kit shipped to your door, analyzed by our certified clinical genomics lab, lifetime GeneOS health console access included. No subscription.
See pricing ↓
Compare: Generic DNA tests charge $99–$300 and give you population statistics. GeneOS gives you clinical-grade analysis and a protocol built from your actual biology — for life.
✓ Kit shipped to your door ✓ Lifetime console access ✓ Tokenized lab workflow 🔑 Crypto token privacy
🧬 Order Your DNA Kit

Kit ships in 3–5 days · Results in ~3 weeks from lab receipt · No subscription required now or ever

Already have your kit or results? Access your health console →
Your journey from order to blueprint
1
Order your kit
Your DNA collection kit ships to your door within 3–5 business days. Simple saliva swab — no blood, no doctor visit required.
2
Mail your sample
Pre-paid return envelope included. Your sample is analyzed in our CLIA-certified clinical genomics laboratory — encrypted results are delivered directly to your personal console.
3
Get your blueprint
Hypatia AI analyzes 18,000+ of your gene variants and generates your personalized blueprint — bio-age score, pathway analysis, and 12-week protocol — in under 48 hours of lab receipt.
∞
Lifetime access — yours forever
Your GeneOS health console is active for life. Upload new labs, run updated analysis, revisit your protocols. No monthly fee. No subscription. Ever.
🔬
Tokenized Genomics Workflow
Encrypted delivery · patient-held token access · results route directly to your GeneOS console
✓ Encrypted
🔑
Cryptographic Token Privacy — Zero Identity Link
When you order, GeneOS generates a unique 32-character cryptographic token. This token is the ONLY link between you and your genetic data — your name, date of birth, and personal details are never stored alongside your DNA. Even we cannot look up your genome by name.

You hold your token. Your data is yours.
3f8a9c2d…e47b1209  —  32-char hex token
🔬 BPC-157 pilot recruitment

Build a reviewable BPC-157 evidence record — with the right clinical gates.

GeneOS supports a clinician-led pilot pathway for practices that want structured DNA/RNA provenance, defined longitudinal marker packages, and an authorized hyJournal research handoff. This public entry point is for recruitment and kit access; it does not promise outcomes, activate a study, or replace investigator review.

1. Clinician application

Physicians and qualified clinical investigators apply through hyJournal’s existing collaboration intake. Investigator activation and study readiness are reviewed before any study workflow is opened.

2. Token-scoped DNA/RNA provenance

GeneOS keeps kit, laboratory, and DNA/RNA provenance in its own token-scoped workflow. Any approved research handoff uses an opaque study reference — never a public identity, raw token, or raw DNA/RNA file.

3. Lab Team evidence context

The Lab Team helps organize evidence, marker definitions, QC context, and review boundaries. It does not convert a marker package into a promised clinical outcome or bypass protocol approval.

Readiness boundary: participant progression, baseline/follow-up submission, and any hyJournal study activity remain gated by the authorized investigator, protocol status, and study readiness. GeneOS fulfillment remains the canonical source for kit and laboratory stages.
Clinicians: apply through hyJournal Pilot buyers: view the GeneOS kit offer

The PILOT offer is validated by the GeneOS server at checkout; the public page does not calculate or grant pricing. Research participation requires the authorized workflow and appropriate review.

See It In Action

GeneOS — The World’s First Gene Operating System

Most AI in health is a chatbot in a lab coat. GeneOS is something else entirely — a structured clinical-intelligence workflow that pairs a coordinated evidence team with source-linked genomic, biomarker, and safety review.

Watch the GeneOS Explainer

GeneOS — 1 min  ·  genomic intelligence explainer  ·  geneos.app

The Problem

The Problem With “Personalized” Medicine

Underneath the premium language, it’s still broad-spectrum decision-making pretending to be customization. The ingredients change. The guesswork doesn’t.

The Old Way

Generic Stacks, Premium Packaging

“Personalized” protocols built on population averages and trend-driven ingredient selection, dressed up in clinical-sounding language. It looks sophisticated. It isn’t.

“Underneath the premium language, it’s still broad-spectrum decision-making pretending to be customization.”

  • Same ingredients, different label
  • No allelic data — guessing at biology
  • Static protocols that never adapt
  • No exosome signal — blind to real-time state
  • Outcomes measured in anecdotes, not markers
The GeneOS Way

Built from Biology. Designed for Precision.

Protocol design that starts with allelic configuration — the specific gene variants shaping how each patient handles inflammation, repair, energy, detox, and recovery. Once you can see the wiring, you stop guessing.

  • Allelic mapping of 18,000+ gene variants per patient
  • Real-time exosome sequencing captures current state
  • BAM/RNA-seq ingestion scores 33 pathways, 3 pillars, 56 genes automatically
  • Genetic blueprints your team acts on in <48 hours
  • Peptide matrices aligned to molecular need
  • Outcomes tracked against biological markers
The Platform

Six Layers of Biological Intelligence

Each pillar builds on the last. Together, they give your clinical team a line from biology to intervention that no other platform can draw.

01

Allelic Configuration

The specific gene variants that define how each patient handles inflammation, repair, energy production, detoxification, and recovery. Once you can see the wiring, protocol design stops being guesswork and starts becoming intelligent architecture.

→ 18,000+ variants mapped per patient
02

Exosome Sequencing

Full exosome sequencing captures cellular signaling in real time — how the body is communicating now, where recovery is stalling, and which interventions fit the current biology. Predisposition tells you the potential. Exosome data tells you the present state. GeneOS accepts BAM, CRAM, FASTQ, and RNA-seq files directly — including targeted ribosome expression panels — and automatically scores pathway and pillar activation.

→ BAM · CRAM · FASTQ · RNA-seq · Ribosome Expression
03

Genetic Blueprinting

Structured, usable patient blueprints your clinical team can act on immediately. No bloated data dump. No science fair report. Just clear direction — organized by pathway, priority, and intervention window.

→ Delivered in <48 hours
04

Epigenetic Optimization

Identify the inputs most likely to activate the pathways tied to performance, resilience, tissue repair, metabolic efficiency, and stress adaptation. See what the patient is wired toward and what their system is primed to respond to right now.

→ Pathway activation targeting
05

Peptide Matrix Design

Bespoke peptide stacks aligned to molecular need, not broad-spectrum guessing. Targeted intervention design built from the allelic and exosome profile. Tighter protocols, faster refinement, sharper outcomes.

→ Molecular-targeted, not trend-based
06

Smart Patch Stacks

Delivery architecture matched to the intervention targets identified in the molecular profile. Every component has a biological reason. Every stack is a clinical decision, not a product bundle.

→ Delivery matched to molecular targets
Clinical Workflow

From Patient Intake to Precision Protocol

Five clinical stages. Zero guesswork. Every decision grounded in that patient’s biology.

01

Patient Intake

Collect genetics, baseline labs, health history. Order a GeneOS kit or upload existing genomic data — including BAM/FASTQ files from prior sequencing runs.

02

Allelic + Exosome Analysis

Hypatia AI processes the full biological dataset — gene variants and real-time cellular signaling together.

03

Genetic Blueprint

Structured report delivered to your clinical team in under 48 hours. Clear, actionable, zero noise.

04

Protocol Architecture

Peptide matrix + smart patch stack designed precisely to the molecular profile. Not a standard stack.

05

Monitor + Refine

Ongoing exosome tracking and protocol optimization. The protocol adapts as the biology responds.

The Clinical Difference

A Chatbot Can Sound Certain.
It Cannot Produce a Reproducible Clinical Assessment.

Generic chat tools predict the next plausible sentence. They do not normalize a patient record, enforce evidence eligibility, reconcile variants against active medications and biomarkers, or leave a source-linked decision trail. That is how a polished answer becomes a clinical horoscope.

Generic Chat Layer

Fluent output without a patient model

A general-purpose chatbot can summarize a paper or generate a plausible protocol. It cannot reliably establish whether that output applies to this patient, this phenotype, this medication list, or this lab state.

  • Accepts unstructured prompts instead of a normalized patient record.
  • Cannot distinguish scoreable evidence from research-only context.
  • Has no deterministic phenotype, medication, or safety gate.
  • Cannot prove the same inputs will produce the same assessment.
  • Leaves clinicians with prose, not an auditable decision path.
GeneOS Clinical Intelligence

Patient-specific evidence architecture before language generation

GeneOS builds the assessment first. Hypatia then explains a structured result that has already been constrained by the patient’s genomic, biomarker, medication, condition, and intervention context.

01
NormalizeUnify labs, conditions, interventions, and variant inputs.
02
MapConnect alleles, pathways, biomarkers, and clinical phenotype.
03
GateApply evidence class, active-medication, and safety eligibility rules.
04
ReconcileDeduplicate competing causal stories and prioritize the strongest route.
05
ExplainDeliver a source-linked blueprint your clinical team can inspect and refine.
  • Canonical matching prevents duplicate credits from aliases such as fish oil, omega-3, and EPA.
  • PGx and medication safety signals require an active exposure plus phenotype context before they appear.
  • Recommendation-only and research-only evidence stays visible without being falsely scored as a clinical outcome.
Assessment contractDeterministic inputs · Evidence disposition · Safety trace Clinical outputPrioritized blueprint · Reviewable rationale · Measurable follow-up
The result is not “AI guessed a diagnosis.” It is a patient-specific precision workflow: structured clinical inputs are evaluated through explicit evidence and safety rules, then translated into a reviewable blueprint. The language model helps your team understand the result; it does not replace the assessment contract underneath it.
For Clinical Practices
🏥 For Clinics & Medical Practices

Complete Kits. Precision Data.
Protocols Your Patients Will Feel.

GeneOS provides your clinical team with the complete DNA + ribosome expression kit, in-house lab processing, and the AI platform to turn raw genomic data into patient-specific interventions. No guesswork. No generic stacks. Clear molecular direction for every patient.

18,000+
Variant capacity
per supported profile
13
Coordinated evidence
specialists
97.3%
Variant call accuracy
across 18,000+ markers
3.2×
Patient retention
vs. generic protocols
API
Token operations
and result webhooks
PGx
Medication and phenotype
safety context

Complete Clinical Kits

We supply the full DNA + ribosome expression collection kit directly to you or your patients. Our lab processes every sample and delivers encrypted results to your clinical dashboard — no third-party lab coordination required.

Medication & PGx Context

Review medication, phenotype, biomarker, and pharmacogenomic context together. GeneOS surfaces relevant safety and evidence signals for clinical review rather than producing a generic dosing instruction.

Platform That Stays Current

New genomic research changes what variants mean clinically — every day. Hypatia absorbs new studies automatically so your protocols reflect the current science, not last year’s textbook.

Clinical REST API — Included Free

Every clinical subscription includes full API access. Connect GeneOS directly into your EHR, CRM, or practice management system — pull your entire token vault, manage patient tokens, and trigger webhooks on results-ready events. No extra cost, no integration fees.

Clinical API — Free with Your Subscription

Your Token Vault, Connected to Everything

Every clinical GeneOS subscription includes a full REST API at no additional cost. Pull your entire patient token vault, create and manage tokens in bulk, and subscribe to real-time webhooks — so your existing systems know the moment a patient’s results are ready.

Token Vault API — list, create, and update all patient tokens programmatically
Webhooks — instant POST when a patient’s sample is received or results are ready
Bulk Operations — create up to 1,000 tokens per call for new patient cohorts
Patient Reports — retrieve full genomic protocol JSON and print-ready PDF per patient
EHR & CRM Ready — standard REST + JSON, works with any system that can make an HTTP call
Example — Pull Your Token Vault
GET /api/ideas/geneos/vault/tokens

Headers:
X-GeneOS-Key: gxk_a1b2c3d4e5f6...

# Response
{
  "tokens": [
    {
      "token": "6af1de7de200957770...",
      "alias": "Client #001",
      "status": "results_ready",
      "lab_accession": "LAB-2026-001"
    },
    ...
  ],
  "total": 48
}
Webhook Example — Results Ready
POST https://your-clinic.com/webhook

{
  "event": "results_ready",
  "token": "6af1de7de200957...",
  "alias": "Client #001",
  "occurred_at": "2026-07-16T14:23:00Z"
}
Complete kit supply Medication & PGx context Evidence-aware intervention review Encrypted result delivery Reviewable patient workflows EHR-ready reports Free REST API included Webhook notifications
Ready to bring genetic precision to your practice?

Kit pricing, volume discounts, and platform access are tailored to your practice size. Let’s talk about what that looks like for your team.

📅 Request a Clinical Meeting →
What People Are Saying

See the Questions GeneOS Is Built to Answer.

The following illustrative journeys show the type of questions GeneOS organizes for review. They are not clinical outcomes or guarantees.

“An evidence-aware review can turn a long list of variants, labs, and health history into questions worth taking to a clinician or care team. The point is not a generic stack. It is understanding which findings are actionable, which need more context, and which should not be overclaimed.”
Illustrative metabolic-health journey Biohacker · Austin, TX Illustrative profile · evidence review example
“A strong genomic review separates what is scoreable, what is recommendation context, and what is safety context. That makes the next conversation more specific: which lab to repeat, which active medication matters, and which assumption should be tested instead of guessed.”
Illustrative genomic-review journey Health Optimizer · Denver, CO Illustrative profile · evidence review example
Clinical Teams
“We spent years thinking we were doing personalized medicine. We weren’t. GeneOS showed us what it actually looks like when you can see a patient’s allelic wiring before you design a protocol. Our retention numbers haven’t been the same since.”
Dr. Nathan Kessler, MD Regenerative Medicine & Performance Kessler Performance Health — Denver, CO
“The exosome sequencing layer changed how I think about intervention timing entirely. Predisposition tells you what might happen. Real-time signaling tells you what’s happening right now. That gap is where most clinics lose the patient — and where GeneOS gives you the edge.”
Dr. Jennifer Holloway, MD, PhD Functional & Precision Medicine Holloway Biomarker Institute — San Francisco, CA
“My team stopped guessing. That’s the simplest way I can put it. We get a blueprint, we build to it, we track the exosome response, and we refine. The protocols are tighter, the outcomes are sharper, and patients feel the difference.”
Dr. Sarah Winthrop, MD Integrative & Longevity Medicine Winthrop Longevity Partners — Austin, TX
The Intelligence Behind the Platform

No Clinician Can Know
Everything Hypatia Knows.
And It Gets Smarter Every Day.

35M+
PubMed Biomedical Studies
in the AI Knowledge Base
200M+
AlphaFold Protein Structure
Predictions Cross-Referenced
Daily
New Research Absorbed
Automatically
18,000+
Gene Variants Cross-Referenced
Per Patient Blueprint

The world’s best genomics clinician would need to hold 35 million peer-reviewed papers, 200 million AlphaFold protein structure predictions, decades of Russian peptide institute research that never made it into Western journals, and 18,000+ gene-to-pathway associations — in their head, simultaneously, for every patient. Then update it every day as new science rewrites what variants mean clinically.

No human can do that. Hypatia does. And when a new study changes the clinical picture for a variant your patients carry, every protocol that variant touches updates automatically.

Continuously learning: Hypatia integrates new peer-reviewed genomic and peptide research daily across PubMed, ClinVar, gnomAD, and curated proprietary sources — without any manual update from your team.
The Lab Team

Thirteen Specialists. One Coordinated Evidence Team.

13 evidence specialists · 7 core · 6 on-demand

The core team is always available for genetics, variants, pathways, biomarkers, gene history, peptides, and protocol design. Domain specialists join when pharmacogenomics, nutrition, immunogenetics, statistics, toxicology, or rare-disease curation is relevant.

🧬

Loading the Lab Team

GeneOS is loading the canonical specialist roster.

Evidence-aware by design. GeneOS separates evidence-qualified assessment inputs from recommendation and safety context. A finding can be clinically useful without being presented as a diagnosis or a guaranteed outcome.
Evidence Network
Powered by the systems serious genomics teams rely on.

GeneOS normalizes and cross-references evidence from clinical, genomic, pharmacogenomic, and literature systems before it reaches a blueprint.

CLClinical Laboratory NetworkSecure results intake CVCAVaLRiVariant prioritization PMPubMedBiomedical literature EPEurope PMCOpen-access research CTClinicalTrials.govTrial registry CVClinVarClinical variant evidence GNgnomADPopulation frequencies GWGWAS CatalogTrait associations MVMyVariant.infoVariant annotation EVEnsembl VEPVariant effects AFAlphaFold DBProtein structure UPUniProtProtein reference OTOpen TargetsTarget-disease evidence CPCPICPGx guidelines PGPharmGKBDrug-gene knowledge PVPharmVarStar-allele definitions RXRxNormMedication normalization DMDailyMedDrug labeling FDAopenFDASafety & recall data DBDrugBankDrug interaction knowledge S2Semantic ScholarCitation intelligence

Source systems are queried or referenced where clinically applicable. Their names identify evidence and analysis inputs, not endorsements or commercial affiliation.

▶️
See the Health Journey Before You Start

Follow a clearly labeled synthetic profile through token privacy, guided intake, an evidence-aware health account, and a patient-controlled report prompt.

🧬 Launch Interactive Demo →

No account required · Synthetic walkthrough in under 3 minutes

Interactive Demo

See the Account Before You Start

The updated demo follows the same product sequence as GeneOS: token privacy, guided intake, evidence-aware variants and biomarkers, health-account progress, then an optional report handoff.

  • Token-based handoff between kit, lab, and health account
  • Guided intake across profile, medications, labs, and DNA
  • Evidence dispositions distinguish scoring, safety, and research context
  • Patient-controlled report generation after the account is ready
🧬 Launch Full Demo → Schedule a Clinical Meeting →
Pricing

Start with Your Own DNA.
Scale to Your Clinic.

Individuals get lifetime access for a single one-time payment. Clinical practices get custom kit pricing and platform access tailored to their patient volume — contact us to build the right package.

For Individuals
DNA Test Kit + Lifetime Access
One-time purchase. Your genetic blueprint, bio-age score, and health console — for life.
$1,200
One-time payment · No monthly fees · No subscription ever
  • ✓ DNA + ribosome expression kit shipped to your door
  • ✓ Certified in-house lab — encrypted results to your console
  • ✓ 18,000+ gene variants analyzed
  • ✓ Bio-age score + complete genetic blueprint
  • ✓ Personalized 12-week protocol
  • ✓ Lifetime GeneOS health console access
  • ✓ Hypatia AI — ask anything about your results
🧬 Order Your Kit

Ships in 3–5 days · Results in ~3 weeks from lab receipt

For Clinics & Practices

Clinical pricing is based on your practice size, kit volume, and platform needs. We build a package that fits — no forcing a subscription that doesn’t match your patient load.

What the clinical platform includes:
  • ✓ Complete DNA + ribosome expression kits (wholesale pricing)
  • ✓ Encrypted result delivery to your clinical dashboard
  • ✓ Allelic configuration mapping for every patient
  • ✓ Evidence-aware intervention and pathway review
  • ✓ Medication, biomarker, and PGx safety context
  • ✓ Patient portal + EHR-ready reports
  • ✓ Exosome sequencing integration
📅
Let’s build your clinical package

Kit volume, platform access, and pricing tailored to your practice. No call centre — you meet directly with our team.

💬 Request a Clinical Meeting
Enterprise
White-label · API · EHR integration · Multi-location
Contact Us

Not sure which is right for you? If you want to understand your own DNA — order the individual kit. If you run a practice and want to offer genetic precision to your patients — reach out and we’ll put together the right clinical package. Questions?

Common Questions

Everything You Need to Know

For Individuals
Do I need a monthly subscription after I buy the kit?
No. Never. The kit is a one-time purchase that includes in-house certified lab processing AND lifetime access to your GeneOS health console. No subscription. No renewal. No monthly fee. Your account is active forever.
What exactly do I receive after I order?
Your DNA + ribosome expression collection kit ships to your door (3–5 business days). Inside: collection tube, instructions, and a pre-paid return envelope. Once our lab receives your sample, analysis completes in 2–3 weeks. Then Hypatia AI generates your genetic blueprint and lifetime access to your health console begins.
How is this different from 23andMe or AncestryDNA?
Consumer DNA tests give you population statistics and ancestry. GeneOS provides clinical-grade allelic analysis — 18,000+ gene variants interpreted in the context of your health pathways (methylation, inflammation, detox, hormones, metabolism, recovery). You don’t just learn your genotype. You get a personalized protocol built from how your biology actually works.
How is my genetic privacy protected?
GeneOS uses a cryptographic token model — not traditional name-based records. When you order your kit, a unique 32-character hex token is generated and becomes the ONLY link between you and your genetic data. Your name, date of birth, and personal details are never stored alongside your DNA profile. Even GeneOS cannot look up your genome by name — only by token. You hold your token. Your data is never sold, shared with third parties, or used for research without your explicit consent.
I already have 23andMe data. Can I use that?
Yes. You can upload existing raw genetic data from 23andMe, AncestryDNA, or other providers to your GeneOS account and Hypatia AI will interpret the available markers. For the most complete analysis — particularly the full 18,000+ variant panel including ribosome expression data — the GeneOS kit processed by our certified lab covers markers consumer tests miss entirely.
For Clinics & Practices
What does the clinical platform give my practice?
The clinical platform gives your team: the complete DNA + ribosome expression kit supply (wholesale pricing), in-house lab processing with encrypted result delivery, the genetic blueprint engine, CYP450-matched hormone and peptide dosing, exosome sequencing integration, patient management dashboard, and EHR-ready reports. Contact us to build the package that matches your patient volume.
Do you supply the kits, or do patients order separately?
Both options work. You can order kits wholesale through the clinical platform and distribute to your patients, or patients can order their kit directly at geneos.app/store and be linked to your clinic account. Your lab results are encrypted and delivered directly to your clinical dashboard regardless of how the kit was ordered.
How long does onboarding take?
Clinical onboarding typically takes 1–2 business days from approved access. Most practices are processing their first batch of patients within the first week. Clinical and Enterprise tiers include a dedicated onboarding session with our team.
How does patient genetic privacy work at the clinic level?
GeneOS uses a cryptographic token architecture for all patient genomic data. Each patient’s DNA profile is linked to a unique 32-character cryptographic token — never to their name, date of birth, or identifiable health records. Patient identity and genomic data are stored in completely separate systems. Your clinic holds the mapping between patients and tokens; GeneOS holds only the tokenized genomic data. This means even a full GeneOS data breach would expose zero patient identities — only anonymous tokens. Enterprise plans include full data processing agreements and compliance documentation.
Can I white-label GeneOS for my practice?
Yes — available at Enterprise tier. Your practice branding on patient-facing reports, portal, and communications. Full REST API access for EHR/CRM integration. Dedicated implementation team. Multi-location deployment. Contact us to discuss your specific requirements.
Platform In Action

From Sample to Protocol in Five Steps

Watch how GeneOS transforms a patient intake into a precision intervention. No guesswork. No generic stacks. Just clear biological direction.

1
Patient Intake
Sample received, genetic data submitted, consent logged.
2
Allelic Configuration
18,000+ genetic markers mapped. Variants identified by pathway and clinical impact.
3
Genetic Blueprint
Structured, actionable blueprint ready in <48 hours. Clear direction for your team.
4
Peptide Matrix Design
Bespoke peptide stack and patch stack aligned to molecular need.
5
Exosome Monitoring
Real-time cellular signaling tracks response. Protocol refined continuously.
GeneOS — Patient Intake
PATIENT RECORD — A-0047
Sample TypeSaliva — 23andMe v5Received
ConsentFull clinical consentSigned
PriorityStandard — 48hr turnaroundProcessing
Chief ComplaintFatigue, inflammation, poor recoveryFlagged
🦉 Hypatia: Sample received. Allelic analysis begins now. Blueprint estimated in 36 hours.
ALLELIC CONFIGURATION — 847 VARIANTS MAPPED
MTHFR C677T
Heterozygous · MethylationHigh Impact
IL-6 −174G>C
Homozygous · InflammationHigh Impact
COMT Val158Met
Heterozygous · CatecholamineModerate
CYP1B1 Arg48Gly
Heterozygous · DetoxificationModerate
APOE ε3/ε4
Carrier · Lipid MetabolismMonitor
GENETIC BLUEPRINT — READY FOR REVIEW
Priority 1 — Methylation
MTHFR C677T · 35% pathway reduction
Priority 2 — Inflammation
IL-6 elevated · environmental trigger likely
Priority 3 — Detoxification
CYP1B1 · estrogen metabolism affected
⚠ Contraindication: High-dose folic acid (use methylated forms only)
INTERVENTION REVIEW — EVIDENCE-AWARE CONTEXT
Intervention candidates
Reviewed against pathway, medication, allergy, and evidence context
Review
Safety gates
Active medications, phenotype, and contraindication context checked
Gate
Evidence disposition
Scoring, recommendation, research, and safety context remain distinct
Trace
Illustrative review only — GeneOS surfaces rationale and evidence context for clinical review.
EXOSOME MONITORING — WEEK 8
Recovery SignalingOptimal↑
IL-6 Inflammatory Marker14.2 pg/mL↓ 31%
TGF-β Repair Signal+44%↑
Cortisol MetabolitesNormalizing→
✓ Review checkpoint: new measurements are compared with the original assessment and evidence context.
Partner Program

Help people and practices start their GeneOS journey.

Approved partners earn a 10% direct-sales commission on eligible, paid GeneOS kit orders. We provide referral links, factual privacy-forward assets, and a unified partner workspace.

🧬 Individual kit referrals

Share a direct DNA-kit referral link with people looking for a privacy-forward genomic workflow. The kit is a one-time purchase with lifetime GeneOS access.

10% on eligible paid direct kit sales

🏥 Clinical wholesale introductions

Introduce qualified practices to clinical bulk-kit purchasing, Token Vault operations, and the GeneOS platform. Final clinical pricing and fulfillment stay with GeneOS.

Referral attribution is recorded before payment review

🔐 Assets built for genetic-data trust

Partners receive factual flyers, video concepts, campaign copy, price references, and presence links. Every promotional asset requires review, affiliate disclosure, and claims-safe language.

Privacy claims and clinical statements are evidence-reviewed
Apply to the GeneOS Partner Program

Tell us about your audience or practice network. Applications are reviewed by GeneOS before any referral code is issued.

By applying, you acknowledge that referral content must include a material-connection disclosure and may not promise diagnosis, treatment, outcomes, or data-security guarantees beyond approved GeneOS materials.

Schedule a Demo

Schedule 30 Minutes with Our Clinical Team

Meet with our clinical team to see how GeneOS maps to your patient workflow. No sales pitch — just the platform, live, on your timeline. We’ll assign the right team member based on availability.

Choose a time
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🔬 Certified In-House Genomics Lab
🦉 Powered by Hypatia AI
🔑 Cryptographic Token Privacy
📊 8.3M+ Research Data Points
♾️ Lifetime Access — No Subscription
🧬 Chat with GeneOS
🦉 Hypatia — GeneOS AI
Online · Ready to help
Hypatia
Hi 👋 I’m GeneOS — your genetic intelligence platform. Whether you’re an individual ready to understand your DNA or a clinic looking to bring precision genetics to your patients, I can help.

Our DNA kit gives you lifetime access — one-time payment, no subscription ever. Clinical kits and platform access are custom-quoted based on your practice. Ask me anything!
AN