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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
Manage episode 515189811 series 2631947
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
214 episodes
Manage episode 515189811 series 2631947
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
214 episodes
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