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dc.contributor.authorMiddleton, Annaen
dc.contributor.authorMilne, Richarden
dc.contributor.authorThorogood, Adrianen
dc.contributor.authorKleiderman, Erikaen
dc.contributor.authorNiemiec, Emiliaen
dc.contributor.authorPrainsack, Barbaraen
dc.contributor.authorFarley, Laurenen
dc.contributor.authorBevan, Paulen
dc.contributor.authorSteed, Claireen
dc.contributor.authorSmith, Jamesen
dc.contributor.authorVears, Danyaen
dc.contributor.authorAtutornu, Jeromeen
dc.contributor.authorHoward, Heidi Cen
dc.contributor.authorMorley, Katherine Ien
dc.date.accessioned2019-02-26T11:16:01Z
dc.date.available2019-02-26T11:16:01Z
dc.date.issued2018-11-23en
dc.identifier.issn1878-0849
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/289980
dc.description.abstractWith the use of genetic technology, researchers have the potential to inform medical diagnoses and treatment in actionable ways. Accurate variant interpretation is a necessary condition for the utility of genetic technology to unfold. This relies on the ability to access large genomic datasets so that comparisons can be made between variants of interest. This can only be successful if DNA and medical data are donated by large numbers of people to 'research', including clinical, non-profit and for-profit research initiatives, in order to be accessed by scientists and clinicians worldwide. The objective of the 'Your DNA, Your Say' global survey is to explore public attitudes, values and opinions towards willingness to donate and concerns regarding the donation of one's personal data for use by others. Using a representative sample of 8967 English-speaking publics from the UK, the USA, Canada and Australia, we explore the characteristics of people who are unwilling (n = 1426) to donate their DNA and medical information, together with an exploration of their reasons. Understanding this perspective is important for making sense of the interaction between science and society. It also helps to focus engagement initiatives on the issues of concern to some publics.
dc.description.sponsorshipThis work was supported by Wellcome grant [206194] paid to AM, LF, KIM, RM via Wellcome Genome Campus Society and Ethics Research Group, Connecting Science. We would like to thank the following people from GA4GH for their encouragement and infrastructure support: Peter Goodhand, Julia Wilson, Bartha Knoppers. This work was also supported by Global Alliance for Genomics and Health, with their funding delivered via Wellcome (GA4GH grant, with thanks to Audrey Duncansen). DV acknowledges the infrastructure funding received from the Victorian State Government through the Operational Infrastructure Support (OIS) Program.
dc.languageengen
dc.publisherElsevier BV
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleAttitudes of publics who are unwilling to donate DNA data for research.en
dc.typeArticle
prism.publicationDate2018en
prism.publicationNameEuropean Journal of Medical Geneticsen
dc.identifier.doi10.17863/CAM.37208
dcterms.dateAccepted2018-11-22en
rioxxterms.versionofrecord10.1016/j.ejmg.2018.11.014en
rioxxterms.versionVoR*
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by/4.0/en
rioxxterms.licenseref.startdate2018-11-23en
dc.contributor.orcidMilne, Richard [0000-0002-8770-2384]
dc.identifier.eissn1878-0849
rioxxterms.typeJournal Article/Reviewen
cam.issuedOnline2018-11-23en
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1769721218307316?via%3Dihub#!en


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International