Course summary

You’ll learn how to interpret genomic data and how genomic data can be integrated into mainstream practice for the diagnosis of diseases such as neurological and cardiovascular disorders. You’ll look at the role of genetics in disease and how genomic information can explain disease mechanisms and biology. We’ll also share examples of both common and rare diseases from across the entire healthcare spectrum to demonstrate how to interpret genomic data. All modules studied on this course can also be studied on a modular basis towards your Professional Development (CPD). When you join the course, you become part of an extensive learning community. You’ll connect with students and professionals from diverse backgrounds, creating opportunities for cross-cultural exchange, inter-professional learning and networking that extend beyond the course.