Achieving the first complete sequence of a human genome via the Human Genome Project represents an incredible feat – but it’s just the tip of the iceberg when it comes to unlocking the power of genomics for drug discovery and development. As the scientific community builds on our understanding of genomics, one of the most critical questions becomes, how can we thoughtfully collect and use genetic data to better understand and support the health of all communities, including those who are underrepresented in clinical research. Co-host Maria Wilson sits down with Mark McCarthy, Principal Fellow and Executive Director of Human Genetics, to explore the interplay between genetics, research, and health impact and the potential for more diverse genetic data to reflect the populations of people who experience the diseases we are studying and expand access to quality healthcare for all. This episode is the first in a two-part series dedicated to inclusivity in research.

Read the full text transcript at: www.gene.com/stories/its-personal-inclusive-research-and-precision-medicine