
Sign up to save your podcasts
Or
This week on The Genetics Podcast, Patrick is joined by Madhuri Hegde, SVP and Chief Scientific Officer of Revvity. They discuss Revvity’s advances in ultra-rapid clinical-grade sequencing, opportunities, challenges, and global inequities in newborn screening, and the dilemma of resequencing versus long-term data storage.
Show Notes:
0:00 Intro to The Genetics Podcast
00:59 Welcome to Madhuri
01:52 Rebranding Revvity as a healthcare company
02:51 Advancements in sequencing and Revvity’s projects, including newborn screening tests and clinical ultra-rapid sequencing
12:29 Opportunities and challenges for newborn sequencing and global inequity in access
17:46 Price of sequencing and data storage versus resequencing considerations
21:10 Complexities and nuances of genomic data interpretation
23:28 Rethinking data portability and storage across the lifespan
26:00 Understanding penetrance and population genetics through lifelong sequencing
27:36 Scaling genetic counseling to match advancements and the potential value of chatbots
32:45 The promise of proteomics and translating Olink data to the clinic
34:31 Implementing polygenic risk scores in clinical management
37:12 Transitioning from academia to industry and insights into product development
38:37 Closing remarks
Find out more
Revvity (https://www.revvity.com/)
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
4.8
4343 ratings
This week on The Genetics Podcast, Patrick is joined by Madhuri Hegde, SVP and Chief Scientific Officer of Revvity. They discuss Revvity’s advances in ultra-rapid clinical-grade sequencing, opportunities, challenges, and global inequities in newborn screening, and the dilemma of resequencing versus long-term data storage.
Show Notes:
0:00 Intro to The Genetics Podcast
00:59 Welcome to Madhuri
01:52 Rebranding Revvity as a healthcare company
02:51 Advancements in sequencing and Revvity’s projects, including newborn screening tests and clinical ultra-rapid sequencing
12:29 Opportunities and challenges for newborn sequencing and global inequity in access
17:46 Price of sequencing and data storage versus resequencing considerations
21:10 Complexities and nuances of genomic data interpretation
23:28 Rethinking data portability and storage across the lifespan
26:00 Understanding penetrance and population genetics through lifelong sequencing
27:36 Scaling genetic counseling to match advancements and the potential value of chatbots
32:45 The promise of proteomics and translating Olink data to the clinic
34:31 Implementing polygenic risk scores in clinical management
37:12 Transitioning from academia to industry and insights into product development
38:37 Closing remarks
Find out more
Revvity (https://www.revvity.com/)
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
31,986 Listeners
1,012 Listeners
43,466 Listeners
2,287 Listeners
127 Listeners
125 Listeners
317 Listeners
6,250 Listeners
5,959 Listeners
88 Listeners
31 Listeners
2,143 Listeners
146 Listeners
11 Listeners
428 Listeners