Why "New Horizon" - Our vision

Too many people are living with a rare genetic disease, unable to find answers because complex mutations escape detection by classic genetic tests, including genome sequencing tests. The technology to diagnose many of these cases already exits but is not accessible to patients because implementation costs are too high. So only patients with rather simple mutations can get diagnosed and the rest live their life not knowing what is making them sick.

We combine deep knowledge in DNA sequencing with our commitment to make these new technologies accessible to launch the most comprehensive genome sequencing test in the market. By helping more people reach a positive diagnosis, we will produce critical information needed to push development of new treatments, facilitating a new horizon of discoveries.