Sobre
This professional program provides a technical overview of pharmacogenomics workflows tailored for health system consultancies. It examines the current CRISPR clinical trials landscape and the implementation of data trusts within genomics. Participants will analyze various consent models and review case studies focused on Genomics England and the DeepVariant pipeline. The curriculum concludes with a practical assignment focused on mapping a precision-oncology patient journey to build internal capacity for healthcare delivery innovation within global health systems.
Vista general
CRISPR Trials and Gene Editing Landscape
.3 pasos
Data Governance and Consent Models
.4 pasos
Technical Case Study Analysis
.3 pasos
Precision-Oncology and Capacity Building
.4 pasos
Final Certification
.1 paso
