DiscoverJust Medicine19. Genetic Database Inequities and the Silent Genomes Project
19. Genetic Database Inequities and the Silent Genomes Project

19. Genetic Database Inequities and the Silent Genomes Project

Update: 2024-08-01
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We’re back again with another episode! This week, dive into the world of genetic testing and the genomic divide with expert guest speakers Dr. Wyeth Wasserman and Dr. Anna Lehman:




Did you know that when it comes to genetic testing, you can’t simply use the same reference data for everybody? Different populations of people share different background variations in their genes, so we need good reference data from diverse populations in order for genetic testing to be applicable and useful for each individual. As you may have guessed, this has some pretty big implications for diagnosis and treatment when it comes to those who are poorly represented in large genetic databases. 




Listen in on my conversation with not one, but TWO amazing guest speakers who are doing some pretty game-changing work on the Silent Genomes Project, which aims to reduce healthcare disparities and improve diagnostic success for children with genetic diseases from Indigenous populations. 

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19. Genetic Database Inequities and the Silent Genomes Project

19. Genetic Database Inequities and the Silent Genomes Project

Just Medicine Podcast