Whole genome sequencing captured almost twice as many genetic abnormalities that may be responsible for disease in infants, compared with a standard targeted test, researchers found.
Home / About Us / News Center / Media Coverage / Whole Genome Sequencing Boosts Diagnosis of Rare Disease in Infants
Whole genome sequencing captured almost twice as many genetic abnormalities that may be responsible for disease in infants, compared with a standard targeted test, researchers found.
© 2024 Rady Children's Institute for Genomic Medicine.