Philadelphia Public Health Lab works to identify new variants of COVID-19 Doctors and technicians are working to identify various COVID-19 variants through genome sequencing.

Experts have published a series of recommendations for improving equity of access to whole-genome sequencing (WGS) for children with cancer across the U.K.

GeneDx announces a ultraRapid Genome, offering accelerated genomic insights for neonatal and pediatric patients in as soon as 2 days.

Rady Children's Hospital-San Diego launched Project Baby Bear, the first state-funded program in California to offer rapid whole genome sequencing for newborns who are critically ill.

Effective today, additional health systems can connect via Aura to order GeneDx’s tests including exome sequencing (ES), whole genome sequencing (WGS) and rapid whole genome sequencing (rWGS).

Ultra-low-pass whole-genome sequencing (ULP-WGS) has emerged as a cost-effective method to estimate tumor burden and identify copy number alterations (CNAs) in plasma without prior knowledge of tumor ...

Nucleus is a clinical-grade DNA test that’s focused on delivering the context you need to act on your health data and personalized health recommendations. First, our platform decodes nearly 100% of ...

From identifying predispositions to diseases, to unlocking fitness potential, and creating customized meal plans based on ...