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dc.contributor.authorMilne, Richard
dc.contributor.authorMorley, Katherine I.
dc.contributor.authorAlmarri, Mohamed A.
dc.contributor.authorAnwer, Shamim
dc.contributor.authorAtutornu, Jerome
dc.contributor.authorBaranova, Elena E.
dc.contributor.authorBevan, Paul
dc.contributor.authorCerezo, Maria
dc.contributor.authorCong, Yali
dc.contributor.authorCosta, Alessia
dc.contributor.authorCritchley, Christine
dc.contributor.authorFernow, Josepine
dc.contributor.authorGoodhand, Peter
dc.contributor.authorHasan, Qurratulain
dc.contributor.authorHibino, Aiko
dc.contributor.authorHoueland, Gry
dc.contributor.authorHoward, Heidi C.
dc.contributor.authorHussain, S. Zakir
dc.contributor.authorMalmgren, Charlotta Ingvoldstad
dc.contributor.authorIzhevskaya, Vera L.
dc.contributor.authorJędrzejak, Aleksandra
dc.contributor.authorJinhong, Cao
dc.contributor.authorKimura, Megumi
dc.contributor.authorKleiderman, Erika
dc.contributor.authorLeach, Brandi
dc.contributor.authorLiu, Keying
dc.contributor.authorMascalzoni, Deborah
dc.contributor.authorMendes, Álvaro
dc.contributor.authorMinari, Jusaku
dc.contributor.authorNicol, Dianne
dc.contributor.authorNiemiec, Emilia
dc.contributor.authorPatch, Christine
dc.contributor.authorPollard, Jack
dc.contributor.authorPrainsack, Barbara
dc.contributor.authorRivière, Marie
dc.contributor.authorRobarts, Lauren
dc.contributor.authorRoberts, Jonathan
dc.contributor.authorRomano, Virginia
dc.contributor.authorSheerah, Haytham A.
dc.contributor.authorSmith, James
dc.contributor.authorSoulier, Alexandra
dc.contributor.authorSteed, Claire
dc.contributor.authorStefànsdóttir, Vigdis
dc.contributor.authorTandre, Cornelia
dc.contributor.authorThorogood, Adrian
dc.contributor.authorVoigt, Torsten H.
dc.contributor.authorWang, Nan
dc.contributor.authorWest, Anne V.
dc.contributor.authorYoshizawa, Go
dc.contributor.authorMiddleton, Anna
dc.date.accessioned2022-05-03T13:58:27Z
dc.date.available2022-05-03T13:58:27Z
dc.date.created2022-02-28T09:55:21Z
dc.date.issued2021-05-25
dc.identifier.citationGenome Medicine. 2021, 13 (1), .en_US
dc.identifier.issn1756-994X
dc.identifier.urihttps://hdl.handle.net/11250/2993992
dc.description.abstractBackground: Public trust is central to the collection of genomic and health data and the sustainability of genomic research. To merit trust, those involved in collecting and sharing data need to demonstrate they are trustworthy. However, it is unclear what measures are most likely to demonstrate this. Methods: We analyse the ‘Your DNA, Your Say’ online survey of public perspectives on genomic data sharing including responses from 36,268 individuals across 22 low-, middle- and high-income countries, gathered in 15 languages. We examine how participants perceived the relative value of measures to demonstrate the trustworthiness of those using donated DNA and/or medical information. We examine between-country variation and present a consolidated ranking of measures. Results: Providing transparent information about who will benefit from data access was the most important measure to increase trust, endorsed by more than 50% of participants across 20 of 22 countries. It was followed by the option to withdraw data and transparency about who is using data and why. Variation was found for the importance of measures, notably information about sanctions for misuse of data—endorsed by 5% in India but almost 60% in Japan. A clustering analysis suggests alignment between some countries in the assessment of specific measures, such as the UK and Canada, Spain and Mexico and Portugal and Brazil. China and Russia are less closely aligned with other countries in terms of the value of the measures presented. Conclusions: Our findings highlight the importance of transparency about data use and about the goals and potential benefits associated with data sharing, including to whom such benefits accrue. They show that members of the public value knowing what benefits accrue from the use of data. The study highlights the importance of locally sensitive measures to increase trust as genomic data sharing continues globally.en_US
dc.description.sponsorshipThis work was supported by Wellcome Trust grant [206194] to Society and Ethics Research, Connecting Science, Wellcome Genome Campus.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.ispartofseriesGenome Medicine;13, Article number: 92 (2021)
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectPublic trusten_US
dc.subjectTrustworthinessen_US
dc.subjectGenomic dataen_US
dc.subjectGenomic researchen_US
dc.subjectInternational surveysen_US
dc.titleDemonstrating trustworthiness when collecting and sharing genomic data: public views across 22 countriesen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s). 2021en_US
dc.source.articlenumber92en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1186/s13073-021-00903-0
dc.identifier.cristin2005970
dc.source.journalGenome Medicineen_US
dc.source.volume13en_US
dc.source.issue1en_US
dc.source.pagenumber1-12en_US


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