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dc.contributor.authorTjensvoll, Kjersti
dc.contributor.authorLapin, Morten
dc.contributor.authorGilje, Bjørnar
dc.contributor.authorGarresori, Herish
dc.contributor.authorOltedal, Satu
dc.contributor.authorForthun, Rakel Brendsdal
dc.contributor.authorMolven, Anders
dc.contributor.authorRozenholc, Yves
dc.contributor.authorNordgård, Oddmund
dc.date.accessioned2022-07-05T11:18:20Z
dc.date.available2022-07-05T11:18:20Z
dc.date.created2022-04-22T21:57:04Z
dc.date.issued2022
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/11250/3002735
dc.description.abstractCirculating tumor DNA (ctDNA) analysis has emerged as a clinically useful tool for cancer diagnostics and treatment monitoring. However, ctDNA detection is complicated by low DNA concentrations and technical challenges. Here we describe our newly developed sensitive method for ctDNA detection on the Ion Torrent sequencing platform, which we call HYbridization- and Tag-based Error-Corrected sequencing (HYTEC-seq). This method combines hybridization-based capture with molecular tags, and the novel variant caller PlasmaMutationDetector2 to eliminate background errors. We describe the validation of HYTEC-seq using control samples with known mutations, demonstrating an analytical sensitivity down to 0.1% at > 99.99% specificity. Furthermore, to demonstrate the utility of this method in a clinical setting, we analyzed plasma samples from 44 patients with advanced pancreatic cancer, revealing mutations in 57% of the patients at allele frequencies as low as 0.23%.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleNovel hybridization- and tag-based error-corrected method for sensitive ctDNA mutation detection using ion semiconductor sequencingen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright The Author(s) 2022en_US
dc.source.articlenumber5816en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1038/s41598-022-09698-5
dc.identifier.cristin2018547
dc.source.journalScientific Reportsen_US
dc.identifier.citationScientific Reports. 2022, 12, 5816.en_US
dc.source.volume12en_US


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