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dc.date.accessioned2018-08-10T10:32:34Z
dc.date.available2018-08-10T10:32:34Z
dc.date.created2017-01-30T11:16:58Z
dc.date.issued2017
dc.identifier.citationMeisal, Roger Rounge, Trine Ballestad Christiansen, Irene Kraus Eieland, Alexander Kirkeby Worren, Merete Molton Molden, Tor Kommedal, Øyvind Hovig, Eivind Leegaard, Truls Michael Ambur, Ole Herman . HPV Genotyping of Modified General Primer-Amplicons Is More Analytically Sensitive and Specific by Sequencing than by Hybridization. PLoS ONE. 2017, 12(1)
dc.identifier.urihttp://hdl.handle.net/10852/62842
dc.description.abstractSensitive and specific genotyping of human papillomaviruses (HPVs) is important for population-based surveillance of carcinogenic HPV types and for monitoring vaccine effectiveness. Here we compare HPV genotyping by Next Generation Sequencing (NGS) to an established DNA hybridization method. In DNA isolated from urine, the overall analytical sensitivity of NGS was found to be 22% higher than that of hybridization. NGS was also found to be the most specific method and expanded the detection repertoire beyond the 37 types of the DNA hybridization assay. Furthermore, NGS provided an increased resolution by identifying genetic variants of individual HPV types. The same Modified General Primers (MGP)-amplicon was used in both methods. The NGS method is described in detail to facilitate implementation in the clinical microbiology laboratory and includes suggestions for new standards for detection and calling of types and variants with improved resolution.en_US
dc.languageEN
dc.publisherPublic Library of Science (PLoS)
dc.titleHPV Genotyping of Modified General Primer-Amplicons Is More Analytically Sensitive and Specific by Sequencing than by Hybridizationen_US
dc.typeJournal articleen_US
dc.creator.authorMeisal, Roger
dc.creator.authorRounge, Trine Ballestad
dc.creator.authorChristiansen, Irene Kraus
dc.creator.authorEieland, Alexander Kirkeby
dc.creator.authorWorren, Merete Molton
dc.creator.authorMolden, Tor
dc.creator.authorKommedal, Øyvind
dc.creator.authorHovig, Eivind
dc.creator.authorLeegaard, Truls Michael
dc.creator.authorAmbur, Ole Herman
cristin.unitcode185,15,5,35
cristin.unitnameForskningsgruppen for biomedisinsk informatikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1441001
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS ONE&rft.volume=12&rft.spage=&rft.date=2017
dc.identifier.jtitlePLoS ONE
dc.identifier.volume12
dc.identifier.issue1
dc.identifier.pagecount14
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pone.0169074
dc.identifier.urnURN:NBN:no-65422
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1932-6203
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/62842/1/Meisal_2017_Hpv.pdf
dc.type.versionPublishedVersion


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