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dc.contributor.authorObradović, Jasmina-
dc.contributor.authorJurisic, Vladimir-
dc.date.accessioned2023-10-31T09:09:24Z-
dc.date.available2023-10-31T09:09:24Z-
dc.date.issued2022-
dc.identifier.isbn9788681652015en_US
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/19218-
dc.description.abstractQuick identification of coronavirus was an emergency in the COVID-19 pandemic. The most used diagnostic tools were serologic, rapid antigen tests, as fast, easily applicable, and affordable, but with lower sensitivity. The results were usually confirmed with a reverse transcription polymerase chain reaction. This assay requires proper expertise and robust laboratory equipment. It is further, costly and time-consuming, with restricted application in low-income countries. Even so, it is used as a golden standard, since it has high specificity and sensitivity. The serologic antibody-based assays were also applied during this Covid-19 burden. Their application was able two weeks after the Covid-19 onset since that was the period when antibodies might be detected. Here are briefly presented the advantages and disadvantages of these assays. Meanwhile, the majority of the diagnostic tests were developed, with some of them being automated and highly sensitive, but often costly. The general recommendation is the improvement of the sensitivity of the serologic tests and development of the easily applicable, fast, and accurate diagnostic tests.en_US
dc.language.isoenen_US
dc.publisherSievert Association, Niš, Serbiaen_US
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.sourceRAP Conferenceen_US
dc.subjectCovid-19en_US
dc.subjectRT-PCRen_US
dc.subjectRapid antigen testen_US
dc.subjectRATsen_US
dc.subjectSARS-CoV-2en_US
dc.titleSENSITIVITY AND SPECIFICITY OF THE ASSAYS IN THE COVID-19 PANDEMICen_US
dc.typeconferenceObjecten_US
dc.description.versionPublisheden_US
dc.identifier.doi10.37392/RapProc.2022.14en_US
dc.type.versionPublishedVersionen_US
Налази се у колекцијама:Institute for Information Technologies, Kragujevac

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