Use

GenomeDx ultraRapid is designed to provide the fastest possible genomic diagnosis for critically ill patients (such as neonatal or pediatric intensive care populations) who require immediate clinical answers. It supports detection of sequence variants—including SNVs, indels, intronic and regulatory variants—repeat expansions, structural variants such as CNVs and large rearrangements, and mitochondrial genome variants. The test is intended to inform critical care decision-making when every hour counts.