Introduction to Whole Exome Sequencing (WES): Whole exome sequencing (WES) is utilized when medical and family histories indicate a potential genetic origin for the observed signs and symptoms. It is often performed after previous genetic tests have failed to identify the underlying genetic cause of the patient’s condition. What Is Whole Exome Sequencing? Whole Exome […]

Clinical Exome Sequencing Clinical Exome Sequencing (CES), Often referred to as next-generation sequencing (NGS) for protein-coding genes, Clinical Exome Sequencing (CES) has increasingly become a reliable diagnostic method for identifying unexplained genetic disorders, rare inherited conditions, and other undiagnosed medical syndromes. Therefore, when symptoms fail to indicate a specific diagnosis, Clinical Exome Sequencing serves as