Explore the Power of RNA Sequencing With MOx 2.0
With a complete clinical picture via multiomic data, the process and precision of diagnosing and treating rare diseases is being redefined. By unlocking a deeper understanding of human biological processes at the molecular level with transcriptomics, a revolutionary advancement in the realm of multiomics is being made.
Throughout the webinar, CENTOGENE’s Prof. Peter Bauer, M.D., Chief Genomic and Medical Officer, and Dr. Jorge Pinto Basto, Vice President Medical Genetics, dove deep into the diagnostic challenges which we can now overcome via transcriptomics – utilizing RNA sequencing to enable the analysis of splicing variants and fostering a new era of insights.
What Will You Learn?
- Diagnostic Challenges
- Revolutionizing Precision Medicine
- The Multiomic Approach
- Integrating Transcriptomics
- MOx 2.0 in Action
Prof. Peter Bauer, M.D., serves as CENTOGENE’s Chief Medical and Genomic Officer, where […]
Jorge serves as CENTOGENE’s Vice President Medical Genetics. Bringing in over 15 years […]