Whole Genome Sequencing
Whole Genome Sequencing is a method used for genetic sequencing that analysis your whole genome. It allows us to provide you with Polygenic Risk Scores and other comprehensive analyses on your health based on your own data.
We provide you with access to the most effective tests for personalised and preventative healthcare. We are driven by using the latest research, best-in-class analysis, and most innovative tests to deliver to you a personalised health plan that is created just for you with inputs from leading specialists in their respective fields.
We are driven by using the latest research, best-in-class analysis, and most innovative tests to deliver to you a personalised health plan that is created just for you with inputs from leading specialists in their respective fields.
Whole Genome Sequencing is a method used for genetic sequencing that analysis your whole genome. It allows us to provide you with Polygenic Risk Scores and other comprehensive analyses on your health based on your own data.
Our panel Polygenic Risk Scores analyse more than 39 million genetic positions, to identify an individual’s genetic risk across 27 different conditions. Studies conducted by leading universities in the world have concluded that these results can at times play as much weight in determining one’s lifetime risk of developing a condition as other factors such as lifestyle and environment, smoking, or family history.
Throughout the process, you can always contact your personal Health Custodian to answer any questions.
