Your data. Your choices.
We do not sell your genetic information.
Genetic information is deeply personal. This page explains how it is handled, what you control and what never happens without your say.
We do not sell your genetic information.
Buying a kit does not automatically enrol you in research.
If information must legally be retained, we will explain what, why and for how long.
We explain what we collect, why we need it and who may process it.
Your sample journey
The steps below describe the proposed journey. The laboratory will be named and the confirmed arrangements for transport, storage, retention and destruction will be published before launch.
The laboratory logs the returned kit and confirms it arrived safely.
A unique code connects the sample to your order without your name appearing on the working sample.
Laboratory specialists isolate DNA from your saliva or cheek-swab sample.
The DNA is checked before the markers needed for your chosen kit are analysed.
The laboratory output is compared with appropriate reference data and prepared for your report.
Retention, deletion requests and any optional research use are handled according to your choices and applicable legal requirements.
For communities that have not always been treated fairly by science, healthcare or research, that history is real. Nobody is asked to set it aside here.
That is why everything is being built around plain language, separate consent, data-protection principles and open communication before, during and after you choose to engage.
No buried terms and no assumed consent. You should understand what you are agreeing to before you decide.
Buying a kit, receiving updates and supporting research are different choices. One never automatically includes another.
You decide which optional uses you agree to, and there should always be a clear way to change future permissions.
Research is optional
Research participation is always a separate choice, never a condition of buying a kit or receiving your results.
Buying a kit does not enrol you in research.
Any research opportunity is presented separately, with its own information and consent.
You can say yes or no. Your decision does not affect the service you receive.
Where research access is permitted, direct identifiers are separated and replaced with a research code.
ìmọ̀ is being built around UK data-protection principles, with additional care for sensitive genetic information.
Questions or concerns
If something feels unclear, sensitive or worrying, ask us. You do not need to know the right terms before getting in touch.
Contact us about your data