Our Products

Our market-leading tests are developed using our advanced analytics tool, Centrellis™. This health intelligence platform analyzes and interprets extensive information about known inherited diseases, including related mutations, frequency across populations, and the penetrance and expressivity of genetic changes. Insights from Centrellis inform the design of our tests, which are curated to target the most clinically relevant genes and mutations. Centrellis is continuously updated based on the latest scientific advances, which allows us to rapidly evolve our test offerings and provide meaningful clinical interpretations.

Noninvasive Prenatal Select

A simple blood test for meaningful insight into your baby’s health as early as 9 weeks into pregnancy Learn More

Expanded Carrier Screen

A comprehensive and accurate carrier screen for more than 283 inherited conditions if you’re pregnant or preparing for pregnancy Learn More

CarrierCheck

A simple genetic screen for 67 inherited conditions to help you discover how your DNA could affect your future children Learn More

Natalis Newborn Screen

A simple, at-home test that gives you early insight into your baby’s health by screening for 193 childhood diseases Learn More

Sema4 Signal Oncology Solutions

Sema4 Signal enables and advances precision oncology care, from prevention to treatment to remission Learn More

Test Catalog

Our comprehensive offering of genetic and genomic tests, powered by state-of-the-art technologies Learn More