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Episode 21 – From broad questions to exact answers

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Manage episode 413262843 series 2136231
Content provided by Rare in Common and Cambridge BioMarketing. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Rare in Common and Cambridge BioMarketing or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
With gene therapies on the horizon, a diagnosis is more important than ever. In this installment of the American College of Medical Genetics and Genomics (ACMG) series, our guest Melanie O’Leary discusses the Rare Genomes Project and the goal to use whole genome sequencing technology to find answers for those with undiagnosed genetic diseases. Listen as she explains why broad is better in finding a diagnosis and the importance of partnerships with patients.
  continue reading

29 episodes

Artwork
iconShare
 
Manage episode 413262843 series 2136231
Content provided by Rare in Common and Cambridge BioMarketing. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Rare in Common and Cambridge BioMarketing or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
With gene therapies on the horizon, a diagnosis is more important than ever. In this installment of the American College of Medical Genetics and Genomics (ACMG) series, our guest Melanie O’Leary discusses the Rare Genomes Project and the goal to use whole genome sequencing technology to find answers for those with undiagnosed genetic diseases. Listen as she explains why broad is better in finding a diagnosis and the importance of partnerships with patients.
  continue reading

29 episodes

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