Are you curious how rare disease patients are diagnosed using genetic tests? Dr. Ngu Lock-Hock, Head of Medical Genetics at Kuala Lumpur Hospital, will be joining us as our guest speaker to share rare disease cases. You will hear how 3billion’s technology was applied and played a key role in diagnosis.
Here is what you can expect from our webinar:
- How whole exome sequencing (WES) can be used to diagnose genetically heterogeneous diseases.
- How the WES pipeline and variant interpretation process works at 3billion.
- What the near and distant future of genetic testing for rare diseases may hold.
Interesting Collaborative Cases from Kuala Lumpur Hospital, Malaysia
Ngu Lock-Hock, MD, Ph.D. / Gohun Seo MD, Ph.D.
Rethinking Clinical Practice for Rare Diseases in the Genomic Era
Hane Lee Ph.D.
