Private Genome Action Plan
Spoke DNA sorts your existing DNA file into what looks worth checking, what can wait, and what is only background.
Turn your existing 23andMe, AncestryDNA, MyHeritage, Living DNA, or other supported raw DNA file into a private Genome Action Plan: clear priorities, practical next steps, and careful boundaries around what DNA can and cannot tell you.
Educational, evidence-reviewed reports. Not diagnosis, treatment advice, or a replacement for clinical testing.
Choose Focus if you have one clear question, or Complete if you want the full picture across your genome, context, and priorities.
Single health area
Best for one specific concern.
Full Genome Action Plan
Best balance of depth and price.
Inside a Spoke report
Many DNA reports stop at surfacing associations. Spoke is built to do the harder work after detection: quality-checking, ranking, and prioritising findings by evidence strength, trait importance, personal context, and whether they can responsibly support a next step.
See what gets checked, tracked, discussed, and ignored for now.
Method
Raw DNA can surface thousands of associations. Spoke finds what matters based on evidence strength, trait importance, personal context, and whether the result can responsibly support a next step.
We check file quality and confidence before using a genetic signal.
Scores account for nearby variants travelling together, not just isolated SNPs.
Findings are linked to literature, biomarkers, possible checks, and safety boundaries.
Signals are ranked by relevance, actionability, and what should stay in the background.
FAQ
Privacy, upload, diagnosis, turnaround, and what the report can and cannot do.
No. Spoke does not predict whether you will get cancer, Alzheimer's, or any other condition. Sensitive areas such as cancer context, Alzheimer's, Parkinson's, and psychiatric traits are opt-in only. If you choose to include them, they are handled as limited, non-diagnostic context: clearly labelled, separated from everyday actions, and never framed as a standalone fear-led module.
23andMe, AncestryDNA, MyHeritage, Living DNA, and other raw DNA files we can validate during the fit check. We're adding Nebula and Dante Whole-Genome support in Q3 2026. If you've lost your file, we'll walk you through re-downloading it from your provider.
Focus reports return in 3–4 business days. Complete reports return in 5–7 business days after intake and file checks are complete.
Yes, if that is useful for you. The main report is written for you first: clear priorities, evidence labels, and practical next steps you can act on or track. When a finding is worth discussing, we include a concise clinical summary you can print, save, or attach to your patient portal.
Stored encrypted, used only to generate your report and any updates you request, never sold, never shared with insurers. One click in the portal deletes everything — file, derived data, and report. Receipts of deletion are emailed to you.
No. Spoke reports are educational, designed to inform clinician discussion. Any clinical decision — medication, screening, surgery — requires confirmation through measured tests and a qualified healthcare professional. We say so on every page.
Coming soon
Join the list and we will let you know when the next report places open. No DNA file is needed at this stage.
