How can we, humans, look at our relationship to nature differently? In season three of Going Wild, on top of stories about animals, we invite you to journey through the entire ecological web — from the tiniest of life forms to apex predators — alongside the scientists, activists and adventurers who study it. Wildlife biologist and host Dr. Rae Wynn-Grant has been studying wild animals in their natural habitats all over the world for years. Our award-winning podcast takes you inside the hidde ...
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İçerik Sano Genetics tarafından sağlanmıştır. Bölümler, grafikler ve podcast açıklamaları dahil tüm podcast içeriği doğrudan Sano Genetics veya podcast platform ortağı tarafından yüklenir ve sağlanır. Birinin telif hakkıyla korunan çalışmanızı izniniz olmadan kullandığını düşünüyorsanız burada https://tr.player.fm/legal özetlenen süreci takip edebilirsiniz.
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EP 123: The ethics of newborn genome screening: Actionable insights and beyond with Holly Peay, Senior Research Scientist at the Research Triangle Institute
MP3•Bölüm sayfası
Manage episode 402336895 series 2631947
İçerik Sano Genetics tarafından sağlanmıştır. Bölümler, grafikler ve podcast açıklamaları dahil tüm podcast içeriği doğrudan Sano Genetics veya podcast platform ortağı tarafından yüklenir ve sağlanır. Birinin telif hakkıyla korunan çalışmanızı izniniz olmadan kullandığını düşünüyorsanız burada https://tr.player.fm/legal özetlenen süreci takip edebilirsiniz.
0:00 Introduction
0:50 Holly’s background and career so far
03:30 Complex decision-making and multiple risk factors: Family history, genetics, phenotypes and beyond
07:05 Changes within the last decade to help people make complex, sometimes subjective, healthcare decisions
09:20 Impact on people: The RTI’s mission and the Early Check Study
13:45 Newborn genomic sequencing and the ability to screen for 1000s of conditions with a single dry blood spot
15:40 The ethical translation of new technologies and their integration into complex decision-making
17:00 How parents decide if genomic testing is right for their child
20:46 The factors that play into parents choosing lighter levels of testing rather than more in-depth options
23:25 Actionable insights: Choosing type-1 diabetes as a single newborn genetic screening panel
25:25 The percentage of families that receive an actionable result from the genomic testing process
28:30 Linking screening programmes with clinical trials: How to approach adding new genes to screening panels as research evolves
30:55 The ethical challenges around providing families with opportunities to support clinical trials
33:32 The types of genes included in Early Check’s different newborn screening panels and how they were categorised
36:18 Addressing incomplete genetic penetrance and the non-binary nature of genetic conditions
39:41 Fragile-X: Pre-mutation information and the ethical importance of second consent
41:28 The limitations of using a single blood spot sample and the potential solutions
44:29 Closing remarks
Please consider rating and reviewing us on your chosen podcast listening platform!
164 bölüm
MP3•Bölüm sayfası
Manage episode 402336895 series 2631947
İçerik Sano Genetics tarafından sağlanmıştır. Bölümler, grafikler ve podcast açıklamaları dahil tüm podcast içeriği doğrudan Sano Genetics veya podcast platform ortağı tarafından yüklenir ve sağlanır. Birinin telif hakkıyla korunan çalışmanızı izniniz olmadan kullandığını düşünüyorsanız burada https://tr.player.fm/legal özetlenen süreci takip edebilirsiniz.
0:00 Introduction
0:50 Holly’s background and career so far
03:30 Complex decision-making and multiple risk factors: Family history, genetics, phenotypes and beyond
07:05 Changes within the last decade to help people make complex, sometimes subjective, healthcare decisions
09:20 Impact on people: The RTI’s mission and the Early Check Study
13:45 Newborn genomic sequencing and the ability to screen for 1000s of conditions with a single dry blood spot
15:40 The ethical translation of new technologies and their integration into complex decision-making
17:00 How parents decide if genomic testing is right for their child
20:46 The factors that play into parents choosing lighter levels of testing rather than more in-depth options
23:25 Actionable insights: Choosing type-1 diabetes as a single newborn genetic screening panel
25:25 The percentage of families that receive an actionable result from the genomic testing process
28:30 Linking screening programmes with clinical trials: How to approach adding new genes to screening panels as research evolves
30:55 The ethical challenges around providing families with opportunities to support clinical trials
33:32 The types of genes included in Early Check’s different newborn screening panels and how they were categorised
36:18 Addressing incomplete genetic penetrance and the non-binary nature of genetic conditions
39:41 Fragile-X: Pre-mutation information and the ethical importance of second consent
41:28 The limitations of using a single blood spot sample and the potential solutions
44:29 Closing remarks
Please consider rating and reviewing us on your chosen podcast listening platform!
164 bölüm
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