Children’s hospitals have a unique need to rapidly diagnose genetic diseases
Studies have reported that 34% of children’s hospital admissions had clear genetic underlying disorders that accounted for 50% of the total hospital charges for all admitted patients. If diagnosed rapidly, most genetic illnesses can be easily treated, leading to improved patient outcomes and substantial savings in healthcare costs.
Fabric Genomics helps pediatric hospitals rapidly diagnose genetic diseases through NGS panel testing and whole exome and genome testing.
Watch the Webinar
Kataryzna Ellsworth, PhD FACMG discusses implementation and scaling of rapid genome testing at Rady Children’s Hospital
Fabric Can Support All NGS Testing
What shape does your testing take?
