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EP 210: Live from ASHG: Breaking barriers in genomics with Heidi Rehm of the Broad Institute and Slavé Petrovski of AstraZeneca

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Manage episode 515189811 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics 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://podcastplayer.com/legal.

Summary:

This week on The Genetics Podcast, recorded live at ASHG 2025, Patrick is joined by Heidi Rehm, Chief Genomics Officer at MGH’s Center for Genomic Medicine and Co-director at the Broad Institute, and Slavé Petrovski, Vice President of AstraZeneca's Centre for Genomics Research. They discuss the rapid progress of large-scale genomics, the barriers to integrating genetic data into healthcare and drug development, and how open collaboration, global data sharing, and a focus on equity are driving more inclusive and impactful genomic discovery.

Show Notes:

0:00 Intro to The Genetics Podcast

00:59 Welcome to Heidi and Slavé

02:01 Slavé’s role at AstraZeneca and work in genomics-driven R&D

03:24 Heidi’s work at the Broad Institute bridging clinical genomics, rare disease research, and global data-sharing initiatives

04:12 Heidi on breaking a Guinness world record for rapid neonatal ICU (NICU) genomics and the shift to open data sharing

06:32 Slavé on how large-scale, multimodal human data is transforming genomics research

08:10 Heidi’s initiatives to integrate genomics into routine care at hospitals and with primary care physicians

11:47 Integrating genomics into clinical trials and healthcare, and enabling global discovery through AstraZeneca’s open data portal

15:34 Breaking down legal and logistical barriers to genomic data sharing and centering the patient voice

18:40 AstraZeneca’s large-scale plasma proteome study and machine learning models predicting disease onset years before diagnosis

21:44 Emerging omics tools advancing rare disease diagnosis

24:19 The value and pitfalls of AI in genomics today

28:54 Advancing health equity in genomics through data sharing, diverse recruitment, and global collaboration

33:40 Progress and challenges in next-generation genetic therapies

37:15 Reflections and advice for the next generation entering genomics and data-driven medicine

40:44 Audience Q&A

51:44 Closing remarks

Please consider rating and reviewing us on your chosen podcast listening platform!

https://drive.google.com/file/d/1Bp2_wVNSzntTs_zuoizU8bX1dvao4jfj/view?usp=share_link

  continue reading

214 episodes

Artwork
iconShare
 
Manage episode 515189811 series 2631947
Content provided by Sano Genetics. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Sano Genetics 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://podcastplayer.com/legal.

Summary:

This week on The Genetics Podcast, recorded live at ASHG 2025, Patrick is joined by Heidi Rehm, Chief Genomics Officer at MGH’s Center for Genomic Medicine and Co-director at the Broad Institute, and Slavé Petrovski, Vice President of AstraZeneca's Centre for Genomics Research. They discuss the rapid progress of large-scale genomics, the barriers to integrating genetic data into healthcare and drug development, and how open collaboration, global data sharing, and a focus on equity are driving more inclusive and impactful genomic discovery.

Show Notes:

0:00 Intro to The Genetics Podcast

00:59 Welcome to Heidi and Slavé

02:01 Slavé’s role at AstraZeneca and work in genomics-driven R&D

03:24 Heidi’s work at the Broad Institute bridging clinical genomics, rare disease research, and global data-sharing initiatives

04:12 Heidi on breaking a Guinness world record for rapid neonatal ICU (NICU) genomics and the shift to open data sharing

06:32 Slavé on how large-scale, multimodal human data is transforming genomics research

08:10 Heidi’s initiatives to integrate genomics into routine care at hospitals and with primary care physicians

11:47 Integrating genomics into clinical trials and healthcare, and enabling global discovery through AstraZeneca’s open data portal

15:34 Breaking down legal and logistical barriers to genomic data sharing and centering the patient voice

18:40 AstraZeneca’s large-scale plasma proteome study and machine learning models predicting disease onset years before diagnosis

21:44 Emerging omics tools advancing rare disease diagnosis

24:19 The value and pitfalls of AI in genomics today

28:54 Advancing health equity in genomics through data sharing, diverse recruitment, and global collaboration

33:40 Progress and challenges in next-generation genetic therapies

37:15 Reflections and advice for the next generation entering genomics and data-driven medicine

40:44 Audience Q&A

51:44 Closing remarks

Please consider rating and reviewing us on your chosen podcast listening platform!

https://drive.google.com/file/d/1Bp2_wVNSzntTs_zuoizU8bX1dvao4jfj/view?usp=share_link

  continue reading

214 episodes

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