Revolutionizing healthcare through cutting-edge rare disease testing that aids early detection and paves the way for personalized treatment and improved patient outcomes.
The diagnostic journey for patients can be lengthy, resulting in multiple tests, unclear results, and unanswered questions.
With our technologically advanced solutions, our team of experts provides comprehensive testing programs for detecting clinically significant genomic changes.
We believe that genomic testing is a deep-rooted partnership and are committed to making it accessible and meaningful to the patients and families we serve around the world. Working with physicians, we aim to deliver knowledge that can empower health.
Using a simple saliva or blood sample, we answer complex genetic questions that can proactively inform patient care and help end the diagnostic odyssey for families.
This testing service has not been cleared or approved by the U.S. Food and Drug Administration. Testing services may not be licensed in accordance with the laws in all countries. The availability of specific test offerings is dependent upon laboratory location. The content on this page is provided for informational purposes only, not as medical advice. It is not intended to substitute the consultation, diagnosis, and/or treatment provided by a qualified licensed physician or other medical professionals.
