Question 1: How can we endure that diverse populations are adequately represented in genetic research, and what steps can be taken to address the historical imbalances in the field?
Question 2: In what ways do you think increasing diversity in genetic studies can improve healthcare outcomes for all populations, and how can we measure the impact of that diversity?
Question 3: What ethical considerations should there be when conducting genetic research on diverse populations, particularly in cases where information about ancestry and genetic predisposition to disease could have personal and societal implications?