Whole exome sequencing can identify genetic variants undetected by targeted gene panel testing. In this test-specific episode of our "Answers From the Lab" podcast, Cherisse Marcou, Ph.D., and Kristen Rasmussen, M.S., CGC, explain how our whole exome sequencing reflex test provides cost-effective diagnosis of complex genetic conditions. https://bit.ly/443etSA | Mayo Clinic Laboratories
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NextGenMedic on Instagram: "Exome sequence analysis, also known as whole exome sequencing (WES), is a genetic test that examines the protein-coding regions of DNA called exons, which contain most disease-causing mutations. It helps identify genetic changes responsible for inherited or rare disorders and can guide diagnosis and treatment. The test involves collecting a DNA sample, sequencing the exons, and analyzing the data to detect mutations linked to diseases. #fyp #health #medlife #disease #
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