In neonatal intensive care units across the country, critically ill newborns are in a race against time, while families often wait weeks — or even months — for answers. New research from Tufts Medical Center shows there’s a better way. We explore how rapid whole genome sequencing nearly doubles diagnostic rates in critically ill infants compared to standard testing — and can save the health care system hundreds of thousands of dollars per baby when used early. It’s a powerful example of whole...