Piloting Badger-Seq: a revolutionary paradigm for the genomic diagnosis of critically ill newborns

Awarded in 2024
Updated Apr 24, 2025

At a Glance

Infants born with a rare genetic disorder or birth defect experience high acuity, prolonged hospital stays and a lifetime of health challenges. Molecular diagnosis is key to caring for these infants, and speed is critical. This multidisciplinary team of researchers will use an approach to screening using artificial intelligence and a revolutionary genome sequencing platform to bring state-of-the-art ultra-rapid genome sequencing to infants in hospitals across Wisconsin.