Publication:
Using a web-based application to define the accuracy of diagnostic tests when the gold standard is imperfect

dc.contributor.authorCherry Limen_US
dc.contributor.authorPrapass Wannapinijen_US
dc.contributor.authorLisa Whiteen_US
dc.contributor.authorNicholas P.J. Dayen_US
dc.contributor.authorBen S. Cooperen_US
dc.contributor.authorSharon J. Peacocken_US
dc.contributor.authorDirek Limmathurotsakulen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.contributor.otherUniversity of Cambridgeen_US
dc.date.accessioned2018-10-19T04:28:37Z
dc.date.available2018-10-19T04:28:37Z
dc.date.issued2013-11-12en_US
dc.description.abstractBackground: Estimates of the sensitivity and specificity for new diagnostic tests based on evaluation against a known gold standard are imprecise when the accuracy of the gold standard is imperfect. Bayesian latent class models (LCMs) can be helpful under these circumstances, but the necessary analysis requires expertise in computational programming. Here, we describe open-access web-based applications that allow non-experts to apply Bayesian LCMs to their own data sets via a user-friendly interface. Methods/Principal Findings: Applications for Bayesian LCMs were constructed on a web server using R and WinBUGS programs. The models provided (http://mice.tropmedres.ac) include two Bayesian LCMs: the two-tests in two-population model (Hui and Walter model) and the three-tests in one-population model (Walter and Irwig model). Both models are available with simplified and advanced interfaces. In the former, all settings for Bayesian statistics are fixed as defaults. Users input their data set into a table provided on the webpage. Disease prevalence and accuracy of diagnostic tests are then estimated using the Bayesian LCM, and provided on the web page within a few minutes. With the advanced interfaces, experienced researchers can modify all settings in the models as needed. These settings include correlation among diagnostic test results and prior distributions for all unknown parameters. The web pages provide worked examples with both models using the original data sets presented by Hui and Walter in 1980, and by Walter and Irwig in 1988. We also illustrate the utility of the advanced interface using the Walter and Irwig model on a data set from a recent melioidosis study. The results obtained from the web-based applications were comparable to those published previously. Conclusions: The newly developed web-based applications are open-access and provide an important new resource for researchers worldwide to evaluate new diagnostic tests. © 2013 Lim et al.en_US
dc.identifier.citationPLoS ONE. Vol.8, No.11 (2013)en_US
dc.identifier.doi10.1371/journal.pone.0079489en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-84896706516en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/30952
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84896706516&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleUsing a web-based application to define the accuracy of diagnostic tests when the gold standard is imperfecten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84896706516&origin=inwarden_US

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