Agent-native genomics
Your genes,
operationalized
Grounded in published research. AI agents analyze each variant, cross-reference gene interactions, and translate them into precise recommendations — personalized to your genotype.
$199 one-time fee — early bird pricingWorks with raw data from
Any service that exports standard raw genotype data
Did you know?
Some people can drink coffee at midnight and sleep fine
Two genes work together to determine your actual caffeine response — one controls how fast you clear it, the other how strongly your brain reacts. The combination explains why the same cup hits people so differently.
The supplement aisle sells the wrong form of folate for 40% of people
The supplement aisle sells one form of folate, but a common gene variant means some people convert almost none of it. A simple switch to the right form can change everything for energy, mood, and focus.
18% of people are missing a protein in their fast-twitch muscle fibers
Your muscle fiber composition and fat oxidation profile are shaped by two genes that work in combination. Knowing which way they lean can help you train smarter — not just harder.
Get your personalized action plan
Upload your DNA data and get our library of recommendations filtered by your genotypes.
$199 once — yours forever. Early bird pricing. No subscription.
Specific enough to act on
We’ve distilled thousands of peer-reviewed papers into actionable recommendations for variants and gene interactions.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
Support methylation cycle at multiple points Moderate
Even mildly reduced AHCY efficiency becomes clinically relevant when MTHFR is severely impaired — SAH accumulates faster when methylfolate production is limited.
Aggressively support methylation through multiple pathways Moderate
Impaired MTHFR reduces methylfolate production while impaired AHCY allows SAH to accumulate and inhibit methylation — a double bottleneck creating severe methylation impairment.
MTHFR
AHCY
Ask follow-up questions
The core analysis is deterministic — no AI involved. Your data gets matched against a structured knowledge base and that’s your result. These agents are opt-in layers on top, for when you want to go deeper.
Go deeper
The dashboard gives you starting points. The MCP server lets you pull the thread — with your own AI, on your own machine.
Cross-reference anything
Hand your agent a blood panel, a prescription, a research paper. It reads them alongside your genetic profile and connects the dots — “your ferritin is low, and here’s why your genotype makes that harder to fix.”
Build a personal health library
Not a chatbot you start over each time. Keep notes, save findings, come back weeks later and pick up where you left off. Your understanding compounds.
Nothing leaves your machine
You choose which AI sees your data. Pair the MCP server with a local model and your genetic information never touches the internet.
MCP Server
Connect your own agent
Works with Claude Code, ChatGPT, Cursor, or any MCP-compatible client. Two minutes to set up.
Set up MCPBuilt-in AI agent
Ask anything about your results in plain language. The agent sees your full genotype profile, all your action items, gene interactions, and the research articles behind every recommendation.
- “What should I know about my methylation results?”
- “Which of my variants affect how I metabolize caffeine?”
- “Summarize all my supplement recommendations in one list.”
Uses Claude by Anthropic. Your genetic results and health data are sent to Anthropic’s API for processing. See Anthropic’s privacy policy. For full control over which model processes your data, use the MCP server instead.
Try the agentMCP server — bring your own agent
Securely connect your own AI agent to your health data and our knowledge base via MCP tools (Model Context Protocol) — the open standard for connecting AI agents to external data. Use Claude Code, ChatGPT, Cursor, your own custom agent, or any MCP-compatible client.
Your personal data
Genotype results, action items, risk factors, gene interaction insights
Full knowledge base
556 variants, 4,097 recommendations, research articles, PubMed links
Your agent gets the same data the built-in agent uses — structured, up-to-date, and ready to reason about. Your genetic data never leaves your machine if you pair the MCP server with a local model like Llama or Mistral.
Your file, your rules
You choose exactly what happens to your genome data. Every feature works either way.
Delete after scan
Maximum privacy, zero retention
We parse your file, match your variants against our database, then permanently delete the raw file. Only your matched genotypes are kept — the minimum needed for your personalized results.
When we add new research, we’ll let you know so you can re-upload and get matched to the new variants.
Store encrypted
Always up to date, no re-uploads
Keep your file in your personal account so we can automatically match it against future research — no need to re-upload when we add new variants. New results just appear.
Delete the stored file anytime from your account page. One click and it’s gone.
Your data is never shared with third parties. Processed entirely on our servers in the EU. Delete all your data at any time from your account — no questions asked.
Rigorous methodology
Every article and recommendation in GeneOps is produced by state-of-the-art research agents using the most capable frontier models available, validated against strict schemas.
Deep per-variant research
Each variant is researched individually — clinical databases and published studies reviewed, findings synthesized with evidence-graded recommendations and PubMed citations.
Alleles verified against dbSNP
Every allele is checked against the NCBI dbSNP reference database. Plus-strand orientation, population frequencies, and risk alleles confirmed before any recommendation is written.
Structured and queryable
All output validated against strict schemas — genotype alleles, evidence levels, action types, citations — loaded into a relational database where every fact is cross-referenced.
Continuously expanding
New categories and variants added through orchestrated batch research runs. Store your genome file and new results appear automatically — or re-upload when we notify you of new research.
Start free, upgrade when you’re ready
Upload your genome and explore your results at no cost. Unlock the full action plan for $199.
Free
No credit card required
- Upload and process your genome
- Dashboard with all category profiles
- Genotype results and explanations
- Browse the full knowledge base
- Preview action items (1 per category)
- Weekly newsletter with personalized insights
Lifetime
Early bird pricing — limited availability
One-time payment, yours forever. No subscription, no renewal. All future updates included.
- Everything in Free, plus:
- All action items — supplements, diet, lifestyle, monitoring
- Gene interactions and combined evidence
- Built-in AI agent for follow-up questions
- MCP API for your own AI agents
- Offspring analysis with connections
Browse the research
556 variant articles with genotype interpretations, evidence grades, and PubMed citations. 4,097 recommendations you can read before signing up.
Free and public — no account required.
Explore the knowledge base