DNA Today Podcast: Whole Genome Sequencing and Multiomics Tools Closing the Rare Disease Diagnostic Gap

Despite advances in genetic testing, many patients with suspected rare diseases still spend years searching for answers. In this DNA Today episode, Dr. Christine Eng and Chris Sands of Baylor Genetics discuss how Whole Genome Sequencing, enhanced with technologies like RNA Sequencing, long-read sequencing, and optical genome mapping, is helping providers move beyond single-test approaches to deliver clearer, more actionable diagnoses.

Tune in to the full episode on DNA Today to hear how these advances are helping close the diagnostic gap and what they mean for providers and their patients.