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Can long-read sequencing transform genetic diagnoses?
Manage episode 376434377 series 3400045
PHG Foundation에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 PHG Foundation 또는 해당 팟캐스트 플랫폼 파트너가 직접 업로드하고 제공합니다. 누군가가 귀하의 허락 없이 귀하의 저작물을 사용하고 있다고 생각되는 경우 여기에 설명된 절차를 따르실 수 있습니다 https://ko.player.fm/legal.
Heather Turner, Policy Analyst at the PHG Foundation, explains for you long-read sequencing, its potential applications and how this new technology measures up against traditional short-read sequencing.
Welcome back to Making science work for health, the PHG Foundation podcast that explains the most promising developments in science and their implications for healthcare.
In each episode, host Ofori Canacoo discusses with a PHG Foundation policy analyst, the underpinning science, the ambitions for improving population health and the impact it could have on patients, on society and on the people delivering your healthcare.
If you would like to find out more about what was discussed in this episode, you can find additional information on our website, phgfoundation.org.
Heather recently wrote two briefings on long-read sequencing. Both are freely available: Clinical long-read sequencing and Long-read sequencing: Clinical applications and implementation.
If you have any questions about the topic then you can email us at intelligence@phgfoundation.org.
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