Search
Search
In today’s multiethnic society, genetic disorders previously confined to specific ethnic groups now occur at increasing frequency in broader populations. Based on assumptions about prevalence, traditional carrier screening only targets single gene disorders, according to ancestry or family history. It may not accurately reflect these changing frequencies. Expanded carrier screening by next-generation sequencing (NGS) enables rapid carrier screening research and genetic analysis across a broader range of disorders, crossing ancestries and geographic regions, with a highly accurate and scalable, cost-effective solution.
Hear what your peers are saying about NGS and expanded carrier screening research in our on-demand webinars: