From Genetic Counselling, Ethics, Nursing, Society

How do we ‘do’ consent? Clinical & research models in genomic medicine 100,000 Genomes Project and beyond

Prof Christine Patch will talk through what has been achieved in the “patient choice” process of consent developed during 100k Genomes and reflect on the challenges of creating an ethically robust research ecosystem as a routine part of clinical care.

CATALOGUED UNDER:
Project: Genetic Counselling, Ethics, Nursing, SocietyType: Presentations, Conferences & Public EngagementContributor: Christine PatchKeywords: 100k GenomesconsentCovid-19Genomics EnglandNHSSER Seminar Seriestrustwhole genome sequencing (WGS)

How do we ‘do’ consent? Clinical & research models in genomic medicine 100,000 Genomes Project and beyond

12th August 2020


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Citation:

Patch C (2020). How do we ‘do’ consent? Clinical & research models in genomic medicine 100,000 Genomes Project and beyond. Invited speaker as a part of the Society and Ethics Research Seminar Webinar Series. 12 August. Online

 

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