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What will it take to make clinical genomics part of everyday medicine? Heidi Rehm The first human genome cost $2.7 billion and took nearly 20 years to complete. Labs around the world now sequence genomes everyday for a fraction of the time and cost. Clinical geneticist Heidi Rehm will discuss how researchers and clinicians are working together to leverage all of that data to change the lives of millions of patients and find the causes for some of the rarest diseases. This lecture is presented in memory of Eliana Hechter and is supported by the Eliana Hechter Memorial Fund. Chapters 08:30 Introduction to SFAS and the Eliana Hechter Memorial Lecture 10:16 Formal Program presented by Heidi Rehm 50:00 Q&A Additional websites resources and related videos; Read how Matchmaker Exchange is helping families find diagnoses: https://www.broadinstitute.org/patien... To find out more about the Rare Genomes Project, visit raregenomes.org Learn how seamless data sharing can lead to improvements in human health: • Enabling Federated Discovery, Access, and ... See Justin’s story: • Justin's Odyssey: A journey in rare diseas... Learn about Hannah’s diagnostic odyssey: • Rare Genomes Project: Hannah Tansey’s story