Managing clinically significant findings in research: the UK10K example
Web of Science
AuthorKaye, J; Hurles, M; Griffin, H; Grewal, J; Bobrow, M; Timpson, N; Smee, C; Bolton, P; Durbin, R; Dyke, S; ...
Source TitleEuropean Journal of Human Genetics
PublisherNATURE PUBLISHING GROUP
University of Melbourne Author/sKaye, Jane
AffiliationMelbourne Law School
Document TypeJournal Article
CitationsKaye, J., Hurles, M., Griffin, H., Grewal, J., Bobrow, M., Timpson, N., Smee, C., Bolton, P., Durbin, R., Dyke, S., Fitzpatrick, D., Kennedy, K., Kent, A., Muddyman, D., Muntoni, F., Raymond, L. F., Semple, R. & Spector, T. (2014). Managing clinically significant findings in research: the UK10K example. EUROPEAN JOURNAL OF HUMAN GENETICS, 22 (9), pp.1100-1104. https://doi.org/10.1038/ejhg.2013.290.
Access StatusOpen Access
Recent advances in sequencing technology allow data on the human genome to be generated more quickly and in greater detail than ever before. Such detail includes findings that may be of significance to the health of the research participant involved. Although research studies generally do not feed back information on clinically significant findings (CSFs) to participants, this stance is increasingly being questioned. There may be difficulties and risks in feeding clinically significant information back to research participants, however, the UK10K consortium sought to address these by creating a detailed management pathway. This was not intended to create any obligation upon the researchers to feed back any CSFs they discovered. Instead, it provides a mechanism to ensure that any such findings can be passed on to the participant where appropriate. This paper describes this mechanism and the specific criteria, which must be fulfilled in order for a finding and participant to qualify for feedback. This mechanism could be used by future research consortia, and may also assist in the development of sound principles for dealing with CSFs.
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