Look beyond single gene testing with expanded carrier screening
Carrier screening to detect the presence of heritable genetic defects has been an important element of reproductive health strategies for over 50 years. Until recently, however, the practice has been restricted to a limited number of single-gene tests offered mainly to higher-risk individuals or populations based on race, ethnicity, or ancestry. But the landscape of carrier screening and its role in reproductive health are changing fast.
Please complete this form to download our carrier screening eBook or watch our webinar on the challenges of sequencing SMN1 and SMN2 for spinal muscular atrophy research.
