Should all babies have their genomes sequenced at birth? The question has been hotly debated for the past 15 years. Unlocking the genome’s 3.2-billion-letter code promises understanding of both health ...

Plummeting costs of DNA sequencing technologies are injecting urgency into the longstanding debate over whether to dive deeper into the genomes of more infants — even apparently healthy ones. Experts ...

If you have ever welcomed a new baby into the world, you know the mix of hope and uncertainty that comes with those first days. For decades, newborn screening has been a quiet triumph of public health ...

When federal lawmakers set out to improve the nation's newborn screening programs in 2007, they succeeded in creating grants and increasing the number of conditions tested throughout the country. Yet ...

The state House of Representatives Health Committee has approved legislation adding Duchenne muscular dystrophy and Gaucher ...

Before leaving the hospital, most babies in the United States are screened for multiple genetic, endocrine, and metabolic disorders and conditions. The first part of the screening process consists of ...

Nearly every baby born in the U.S. has blood drawn in the immediate hours after their birth, allowing the baby to be tested for a panel of potentially life-threatening inherited disorders. This is a ...

New sparQ™ Lysis Kit isolates high-quality, double-stranded genomic DNA from DBS punches for PCR-free whole-genome sequencing workflows in less than 50 minutes BEVERLY, Mass., September 30, ...

Two bills that recently passed the state House of Representatives Health Committee with bipartisan support should move quickly through the state Senate and Gov. Josh Shapiro’s office. At the same time ...

The baby in Arkansas seems healthy at birth. Warm, fuzzy skin. A normal weight. But Aiden Cooper can't keep down formula. Don't worry, he's fine, doctors assure his mother as they leave the hospital.