International Case Reviews with Kuala Lumpur Hospital
Webinar | 21. 09. 08
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.
Session
Interesting Collaborative Cases from Kuala Lumpur Hospital, Malaysia
- Speaker
- Ngu Lock-Hock, MD, Ph.D. / Gohun Seo MD, Ph.D.
- Role
- Head, Genetics Department, Hospital Kuala Lumpur / Chief Medical Officer (CMO) at 3billion
Session
Rethinking Clinical Practice for Rare Diseases in the Genomic Era
- Speaker
- Hane Lee Ph.D.
- Role
- Chief Genomics Officer (CGO) at 3billion
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