Join MyOme for a webinar on advancing rare disease diagnostics through innovative genomic approaches. The session will include an overview of MyOme’s rare disease testing portfolio, featuring tools that improve diagnostic yield for unresolved conditions. Guest speaker Danny E. Miller, MD, PhD (University of Washington), will review the use of methylation signatures in genomic diagnostics enabled by long-read sequencing. He will highlight challenges and opportunities of incorporating this information into practice, including its potential to clarify uncertain results and strengthen variant interpretation. Attendees will learn how these emerging technologies can support more precise diagnoses and more informed counseling for families navigating rare disease.
Zoom Link here: https://myome.zoom.us/webinar/register/WN_AjRMYZyyTAiISXUw56UaEA
