Foreseeing health threats and guiding patients with clear DNA insight
Reading millions of clinical papers and the newest science.
One sample. A full read of your genome, a clear map of your risks, and a care plan shaped around you.
By reading the markers written in your genome, we move from one-size protocols to focused, protective care built uniquely around you.
Everything the engine produces lands in one record. Open a protocol to see what it measures, how it works and how fast it comes back.
While you sleep, Genovera reads 2.1 million clinical papers and re-weighs every variant score in your record. Scroll on to look inside.
Six model families power the protocols above, each auditable and explained in plain language. Tap any frame to open it full-screen.
What clinicians, editors and families say about care that starts with your DNA.
“Genovera turns a genome from a file nobody opens into a plan a family can follow.”
“The first precision-care service that explains every score it gives you.”
“Quietly rigorous. The pharmacogenomic alerts alone justify the enrolment.”
Tell us a little about you and a Genovera counsellor will call within one working day to choose your first protocol.