01 / THE CONTINUING RECORD
One place for a report you can inspect, the files behind it, and a clear record of what changes with the evidence.
ACCESS / PRELAUNCH
Sign in to explore the prelaunch account, or open the fictional sample workspace. Sequencing orders, personal reports and file uploads are not open yet.
A fictional preview. No sign-in or personal data is needed.
Google sign-in uses your name and email to create a Whole DNA account. We do not request access to your Google Drive, contacts or genome data. Read the account data notice.
Questions? team@whole-dna.com · Please do not email genetic files.
Welcome to Whole DNA. Your account is active; no genome has been linked.
Whole DNA is in prelaunch. We are finalizing laboratory, privacy, review and delivery terms before accepting samples or genetic files.
Ask about the launchSAMPLE / 001
Findings, evidence, limits, sources and questions sit together. The sample uses invented results; it is not your genome.
↗The planned account joins the report, supported underlying files and a version history. When an interpretation changes, you should be able to see what changed and why. Final scope and continuity terms will be published before enrollment.
There is no kit connected to this account. Here is the journey a member would be able to follow after ordering opens.
Review the test, privacy choices and final terms before a sample is collected.
Register a kit, send the sample and follow receipt by a qualified laboratory partner.
Extraction, sequencing, bioinformatics and quality review, with limitations stated.
Receive the supported files and an interpretation record after review.
See supported changes to interpretation alongside earlier editions.
Illustrative process only. No stage above describes work completed for this account.
The proposed membership brings related questions together. The fictional sample shows the intended editorial standard; the full service scope remains under review.
Drawn from the structure of a comprehensive genome report. These are topic areas, not promises that DNA alone can settle every question.
Owning a report should include a clear way to understand and export supported underlying data.
Sequencer reads and quality scores.
PlannedReads aligned to a named reference genome.
PlannedVariant calls with reference and analysis context.
PlannedMethods, versions and quality information needed to interpret the files.
PlannedThe public sample includes a self-contained report, PDF and discussion brief. It contains no customer's DNA files.
A revised finding should explain the change and keep the earlier view available. That is the update history we are designing.
Sources, evidence level and limits travel with the finding.
A relevant guideline, classification or study may warrant a supported revision.
Keep the earlier text, source and reason for change visible.
Updates are planned within Whole DNA's agreed analysis scope during the life of the service. Final coverage and continuity terms come before enrollment.
See a fictional revision ↗Basic sign-in details for your prelaunch Whole DNA account.
We do not currently accept genetic files or samples through this account. Before enrollment opens, Whole DNA will publish consent, access, retention, deletion and delivery terms.
Read the account data notice ↗