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Rady Team Demos Improved Outcomes, Cost Savings of Rapid Whole Genome Sequencing in NICU


NEW YORK (GenomeWeb) – Researchers at the Rady Children’s Institute for Genomic Medicine have demonstrated that their rapid whole-genome sequencing diagnostic test for infants with unknown but suspected genetic disorders who are in the neonatal intensive care can save babies’ lives and be cost-effective.

April 5, 2018

Doctors Could Help Sick Babies With Rapid Genetic Tests


In August 2016, Amy Jaeger and Robert Supple became the parents of a daughter they named Rylee. Instead of spending their first months with their baby in blissful exhaustion, the new parents were faced with panic — their baby was shaking and spasming, and they didn’t know why. They took Rylee to a number of […]

March 9, 2018

Fast genome tests are diagnosing some of the sickest babies in time to save them

MIT Technology Review

Rylee Supple seemed like a perfectly healthy baby when she was born in August 2016. But after a few months, her parents, Amy Jaeger and Robert Supple, realized something wasn’t right: instead of making normal baby movements, like kicking and grasping, Rylee’s body would shake and spasm.

March 8, 2018

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