From one simple blood test, our team with analyses your entire whole genome, mapping every A, T, C and G that makes up your 3 billion base pairs in your DNA. The information we discover enables your doctor to help you make the best decisions for your treatment. Your core DNA is preserved throughout most of your cells in your body, does not change throughout your life and is specific to each individual. Accurate whole genome sequencing is only required to be done once in your life, allowing us to re-analyse it over time as your health changes. We use the latest in Language processing to extract Disease-Gene and Drug-Gene links from the scientific literature, and transform this into a readable report for your doctors. 

We recommend that you provide us with a GP or specialist referral. This will ensure that your treating clinicians can explain your results and help you make the right decisions for you as well as provide continued care at each stage of your life.

The turn-around time on test results depends on the specific analysis your doctor has requested, your results and report will be available as soon as possible so that we can best support you and your clinician's decision making. Usually a Whole Genome Sequence takes 1-2 months from blood draw to report, however this may be affected by a number of factors. We will share your detailed tracking information throughout the journey for your peace of mind.