Check fit
We confirm your file source, format, and goal before any upload.
Personalized check
Personalized medicine, made considered
Care, fitted to your 23andMe file. Clear about limits.
Private intakeNo public raw DNA upload.
Evidence reviewedPhD-led, evidence focused.
Context-awareYou, not just your genes.
Your 23andMe file can raise useful health questions. The report explains what may matter, what may not, and which questions are worth carrying into a clinician conversation.
1Check fitWe confirm your file source, format, and goal before any upload.
2Add contextShare your family history, labs, and prevention goals so we can tailor insights that matter.
3Receive a reportYou receive a clear, prioritized report with actions and next steps that fit you.
No public uploadYour raw DNA file stays out of your contact-only readiness check.
Fit before paymentWe confirm your file format and coverage before you pay.
4 business daysUsual readiness after secure intake and file checks.
Consent-ledAnalysis only after explicit intake consent
Evidence reviewedFindings are separated by strength and usefulness
Portal deliveryNo report attachments in ordinary email
Deletion supportedRaw file retention is made explicit before upload
NIH · genomics literacyCDC · family historyACMG · secondary findings
Trust firstDesigned for careful decisions, not casual curiosity.
Compatibility firstNo raw file is collected on the public page.
Non-diagnostic by designReports support prevention review, not treatment decisions.
Deletion supportedDNA data handling is explicit before upload.
Your guided path
A calm, guided path from raw data to clarity.
We make sense of your DNA with care and clinical judgement, so you can focus on what matters most: living well, for you.
Boundary-aware review
Private portal workflow
Concierge support every step
Add context
Share your family history, labs, and prevention goals so we can tailor insights that matter.
Context is everythingReceive a report
You receive a clear, prioritized report with actions and next steps that fit you.
Actionable and practicalDNA readiness check
Let's see if your file is a good fit.
This first step is quick and confidential. We check source, format, goals, and whether your request is best supported by our consumer report or needs review by our team before checkout.
Supported first23andMe, Ancestry, MyHeritage, and compatible raw-data exports.
Team review when neededWhole-genome VCF and unusual formats can be checked by our team before payment.
Boundaries up frontWe do not diagnose disease or tell you to start, stop, or change medication.
Your privacy is our priorityWe only collect what is needed to check fit. Your raw data is never collected on this page.
Sample report structure
See the report before you pay.
The report is designed to be read by a person who wants clarity, not another table of variants. Each section states what is known, what is uncertain, and what context would change the interpretation.
Page 1Summary
Priority findings
A short ranked view of the signals most likely to matter for the buyer's stated goal and family-history context.
Page 2Evidence
Confidence and caveats
Findings are separated into established, context-dependent, and exploratory groups so weak signals do not look stronger than they are.
Page 3Action
Questions for review
The output is a bounded set of follow-up questions for self-review or a clinician conversation, not a diagnosis checklist.
What you receive
A report built for decisions, not curiosity loops.
Spoke DNA Reports are useful when a genetic signal needs context. The report starts with what is most actionable, then shows uncertainty and evidence level before any suggested follow-up.
Prioritized signals
A fit check for supported 23andMe text exports before payment.
Limitations stated
Health-related signals explained with confidence language and limitations.
Action map
Questions to take to a clinician when the evidence or family history warrants it.
Compatibility
Clear file support before checkout.
DNA providers differ by file version and marker coverage. The readiness flow makes this visible before the actual upload.
File sourceStatusNotes
23andMe raw dataReadyText export. Older chip versions may have missing markers.
AncestryDNA raw dataReadyText export. Coverage varies by version and ancestry context.
MyHeritage raw dataReadyCSV or text export. Reviewed for marker coverage before checkout.
Whole-genome VCFManual reviewPotentially useful, but file size and annotation needs vary.
No DNA file yetWaitlistWe can follow up when ordering or sequencing support is available.
Method
Context changes what the DNA should mean.
A raw file can contain many signals. A professional report needs to decide which ones are useful for this person, this goal, and this level of evidence.
File and source check
We confirm whether your raw file is compatible before asking for an upload or payment commitment.
Context intake
Your goals, family history, current screening status, and optional labs change which findings deserve attention.
Evidence review
Findings are grouped by confidence and usefulness, with uncertain signals kept visibly separate.
Action map
The report ends with bounded next questions, not diagnosis language or medication instructions.
Pricing
Simple early-customer pricing for personalized reports.
The first release is capped at 50 customers, so each report can be reviewed carefully and delivered with clear next steps.
A quick fit check covering file source, format, goals, and whether the service is a good match before any secure upload.
Start checkA tailored DNA report with evidence tiers, context-aware interpretation, and practical follow-up questions.
Request checkoutSecure intakeEncrypted storage
Human reviewBy Spoke scientists
Tailored guidanceClear next steps, always
Privacy and care
Your genetic data should be handled with care.
Our intake is deliberately guided, not a data grab. We keep payment intent separate from file upload, request consent before analysis, and support deletion requests.
Consent-first
Secure portal
Deletion supported
No raw DNA file in this formThis page only captures fit and contact details.
Consent before analysisActual uploads happen through the secure portal flow.
No casual reuseData handling is limited to report delivery unless separate consent says otherwise.
Deletion requests supportedRetention and deletion are made explicit before upload.
Landing-page variants
Three campaign entry points, one careful checkout path.
Best for people who already downloaded a 23andMe raw-data file and want a more bounded health review.
Raw DNA reportRaw DNA health reportBest for 23andMe, Ancestry, MyHeritage, or compatible raw-data exports.23andMe interpretation23andMe health interpretationBest for people who already downloaded a 23andMe raw-data file and want a more bounded health review.Genome action planGenome action planBest for people who want a practical plan rather than another long list of variants.
FAQ
Answer the trust questions before checkout.
Can this diagnose a condition?
No. The report is prevention and discussion support. It does not diagnose disease, order tests, or tell you to change medication.
Do I upload my DNA file in the readiness check?
No. The public readiness form captures fit and contact details only. Actual uploads happen later through the secure portal after consent.
What if my file is unsupported?
You will be routed to a team review or the waitlist. The purchase path is designed so unsupported files do not become paid reports by accident.
Will the report recommend supplements?
No supplement stack is generated. Where a genetic signal suggests a useful health question, the report keeps it framed as context for review.
Checkout and waitlist
Start with readiness. Pay only when the fit is clear.
The first offer is intentionally constrained: check fit, request a checkout link or next available spot, then upload through the secure portal after consent.