Unlocking the Potential of Whole Genome Sequencing for Diagnosing Genetic Diseases in Newborns – rotviral.com
Whole genome sequencing (WGS) is an innovative technology that is revolutionizing the way genetic diseases are diagnosed in newborns. By unlocking the potential of WGS, doctors are able to identify genetic diseases in newborns with greater accuracy and speed than ever before. WGS provides a comprehensive view of a newborn’s entire genetic makeup, allowing for…