dc.date.accessioned2019-02-22T14:53:57Z
dc.date.available2019-02-22T14:53:57Z
dc.date.created2019-02-22T14:53:57Z
dc.date.issued2014
dc.identifierhttps://hdl.handle.net/20.500.12866/5581
dc.identifierhttps://doi.org/10.1007/s12561-014-9113-5
dc.description.abstractThe standard methods of diagnosing disease based on antibody microtiter plates are quite crude. Few methods create a rigorous underlying model for the antibody levels of populations consisting of a mixture of positive and negative subjects, and fewer make full use of the entirety of the available data for diagnoses. In this paper, we propose a Bayesian hierarchical model that provides a systematic way of pooling data across different plates, and accounts for the subtle sources of variations that occur in the optical densities of typical microtiter data. In addition to our Bayesian method having good frequentist properties, we find that our method outperforms one of the standard crude approaches (the “3 SD Rule”) under reasonable assumptions, and provides more accurate disease diagnoses in terms of both sensitivity and specificity.
dc.languageeng
dc.publisherSpringer
dc.relationStatistics in Biosciences
dc.relation1867-1772
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectMonte Carlo method
dc.subjectperformance
dc.subjectsensitivity and specificity
dc.subjectimmunoassay
dc.subjectreceiver operating characteristic
dc.subjectenzyme linked immunosorbent assay
dc.subjecthealth care planning
dc.subjectsimulation
dc.subjectoptical density
dc.subjectBayesian learning
dc.titleDisease Diagnosis from Immunoassays with Plate to Plate Variability: A Hierarchical Bayesian Approach
dc.typeinfo:eu-repo/semantics/article


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