Ultimate COVID-19 Detection Protocol Based on Saliva Sampling and qRT-PCR with Risk Probability Assessment

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dc.contributor.authorWon, Jounghako
dc.contributor.authorKazan, Hasan Huseyinko
dc.contributor.authorKwon, Jeako
dc.contributor.authorPark, Myungsunko
dc.contributor.authorErgun, Mehmet Aliko
dc.contributor.authorOzcan, Sureyyako
dc.contributor.authorChoi, Byung Yoonko
dc.contributor.authorHeo, Won Doko
dc.contributor.authorLee, C. Justinko
dc.date.accessioned2021-03-30T01:50:30Z-
dc.date.available2021-03-30T01:50:30Z-
dc.date.created2021-03-30-
dc.date.created2021-03-30-
dc.date.created2021-03-30-
dc.date.created2021-03-30-
dc.date.created2021-03-30-
dc.date.issued2021-02-
dc.identifier.citationEXPERIMENTAL NEUROBIOLOGY, v.30, no.1, pp.13 - 31-
dc.identifier.issn1226-2560-
dc.identifier.urihttp://hdl.handle.net/10203/282191-
dc.description.abstractIn the era of COVID-19 outbreak, various efforts are undertaken to develop a quick, easy, inexpensive, and accurate way for diagnosis. Although many commercial diagnostic kits are available, detailed scientific evaluation is lacking, making the public vulnerable to fear of false-positive results. Moreover, current tissue sampling method from respiratory tract requires personal contact of medical staff with a potential asymptomatic SARS-COV-2 carrier and calls for safe and less invasive sampling method. Here, we have developed a convenient detection protocol for SARS-COV-2 based on a non-invasive saliva self-sampling method by extending our previous studies on development of a laboratory-safe and low-cost detection protocol based on qRT-PCR. We tested and compared various self-sampling methods of self-pharyngeal swab and self-saliva sampling from non-carrier volunteers. We found that the self-saliva sampling procedure gave expected negative results from all of the non-carrier volunteers within 2 hours, indicating cost-effectiveness, speed and reliability of the saliva-based method. For an automated assessment of the sampling quality and degree of positivity for COVID-19, we developed scalable formulae based on a logistic classification model using both cycle threshold and melting temperature from the qRT-PCR results. Our newly developed protocol will allow easy sampling and spatial-separation between patient and experimenter for guaranteed safety. Furthermore, our newly established risk assessment formula can be applied to a large-scale diagnosis in health institutions and agencies around the world.-
dc.languageEnglish-
dc.publisherKOREAN SOC BRAIN & NEURAL SCIENCE, KOREAN SOC NEURODEGENERATIVE DISEASE-
dc.titleUltimate COVID-19 Detection Protocol Based on Saliva Sampling and qRT-PCR with Risk Probability Assessment-
dc.typeArticle-
dc.identifier.wosid000624637400002-
dc.identifier.scopusid2-s2.0-85103294066-
dc.type.rimsART-
dc.citation.volume30-
dc.citation.issue1-
dc.citation.beginningpage13-
dc.citation.endingpage31-
dc.citation.publicationnameEXPERIMENTAL NEUROBIOLOGY-
dc.identifier.doi10.5607/en20063-
dc.identifier.kciidART002691106-
dc.contributor.localauthorHeo, Won Do-
dc.contributor.nonIdAuthorKazan, Hasan Huseyin-
dc.contributor.nonIdAuthorKwon, Jea-
dc.contributor.nonIdAuthorPark, Myungsun-
dc.contributor.nonIdAuthorErgun, Mehmet Ali-
dc.contributor.nonIdAuthorOzcan, Sureyya-
dc.contributor.nonIdAuthorChoi, Byung Yoon-
dc.contributor.nonIdAuthorLee, C. Justin-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorCoronavirus-
dc.subject.keywordAuthorCOVID-19-
dc.subject.keywordAuthorSARS-CoV-2-
dc.subject.keywordAuthorSaliva sampling-
dc.subject.keywordAuthorCOVID-19 risk assessment-
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