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Constructing Participation in Genetic DatabasesCitizenship, Governance, and AmbivalenceUniversity of Nottingham This paper discusses the discourse of participation in the context of genetic databases. Focusing on UK Biobank, it suggests that this discourse can be seen as a reflexive institutional response to public ambivalence towards science and expertise. Drawing on empirical evidence from focus groups, I explore how people from various backgrounds constructed and contested two different kinds of participation in UK Biobank. The first relates to people providing research materials to genetic databases and the second to people becoming co-decision makers in these projects. My analysis highlights how focus groups positioned themselves and others in relation to UK Biobank and drew on a variety of discursive repertoires, such as altruism, public ignorance, expertise, and lay empowerment. I conclude that discourses of participation reflect the way people position themselves and others - as experts, publics, patients, or research subjects - in relation to the opportunities and uncertainties of new biomedical research.
Key Words: genetic databases biobanks participation citizenship ambivalence
Science, Technology & Human Values, Vol. 32, No. 2,
172-195 (2007) |
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