Simple. Secure. Built for ongoing discovery. Sequence or upload. Get app-based insights. Keep your genome under your control.
Start here
Join the upload early-access list, or join the waiting list for 30x whole genome sequencing.
For the deepest reports and future reanalysis — get notified when sequencing opens.
Already tested elsewhere? Join upload early access and use the app when upload access becomes available to you. The app is live and currently available through limited early access.
Overview of the process
One simple path — open a step for more detail when you want it.
Join upload early access, or join the waiting list for 30x whole genome sequencing.
Samples are processed through approved partner laboratories where available. Upload is currently available through limited early access. Either path brings your genome into MyDNABank so you can keep it in one secure place.
Your genomic data is encrypted before upload, with clear access controls you can manage in the app.
Your raw genomic file never leaves the controlled environment. Researchers do not receive or download it. Approved analyses run inside controlled environments.
View health insights in the app across areas such as longevity, heart health, nutrition and more.
New insights can appear as science advances. Report depth depends on the quality of your DNA data, and everything remains under your privacy controls.
Approve, decline or revoke future research access from your dashboard.
Set your consent rules, review access requests, and revoke future access at any time. An ongoing approved study is not interrupted. Consent decisions and approved data access are recorded.
Opt in only when you choose — research access is never the default.
Organisations accessing data under commercial research terms are required to provide compensation, unless you explicitly choose to permit access without compensation. Research matching and participation are not guaranteed.
Research sharing stays off until you decide otherwise. You can approve, decline or revoke future access at any time. Ongoing approved studies are not interrupted.
See a clear record of what you approved and when — so access history is easy to review in the app.
Why 30x matters
Selected-marker tests check limited points. 30x whole genome sequencing builds a foundation for deeper reports and future reanalysis.
Selected points only — useful for ancestry and basic traits, but may miss important genetic variation.
Reads across most of your genome and creates a broader genomic record for supported analysis.
Mostly ancestry and a limited set of trait markers — less room for clinical-adjacent categories.
Supports longevity, heart health, medication, nutrition, fitness, family planning, and more.
Often a one-time snapshot — limited foundation when science and report libraries move forward.
Same stored genome, new insights as interpretation improves — still under your privacy controls.
Privacy by design
Your genome stays inside MyDNABank with encrypted storage and clear access controls.