S3.08 Nothing about me without me: involving patients in genomic research

Genetics Unzipped

The Genetics Society에서 제공하는 콘텐츠입니다. 에피소드, 그래픽, 팟캐스트 설명을 포함한 모든 팟캐스트 콘텐츠는 The Genetics Society 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.

5+ y ago 33:19

MP3•에피소드 홈

Research into genetic conditions relies on information from patients and their families, whether that’s detailed health records or genomic data. As the tools and techniques for DNA and data analysis become cheaper and more organisations get in on this fast-growing field, it’s vital to make sure that the most valuable research resource - human lives - doesn’t get overlooked in the rush. In this episode, recorded at the recent Festival of Genomics in London, we find out why it’s so important to make sure that both academic and commercial research studies are done with rather than on participants.

Full show notes, transcript, music credits and references online at GeneticsUnzipped.com

Genetics Unzipped is written and presented by Kat Arney with audio production by Hannah Varrall. This podcast is produced by First Create the Media for the Genetics Society - one of the oldest learned societies in the world dedicated to supporting and promoting the research, teaching and application of genetics.

167 에피소드