About
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.
Overview
CRISPR Trials and Gene Editing Landscape
.3 steps
Data Governance and Consent Models
.4 steps
Technical Case Study Analysis
.3 steps
Precision-Oncology and Capacity Building
.4 steps
Final Certification
.1 step
