dc.contributor.author | Myrmel, Mette | |
dc.contributor.author | Oma, Veslemøy Sunniva | |
dc.contributor.author | Khatri, Mamata | |
dc.contributor.author | Hansen, Hanne Hellerud | |
dc.contributor.author | Stokstad, Maria | |
dc.contributor.author | Berg, Mikael | |
dc.contributor.author | Blomström, Anne-Lie | |
dc.date.accessioned | 2017-12-11T09:30:23Z | |
dc.date.available | 2017-12-11T09:30:23Z | |
dc.date.created | 2017-11-13T11:11:54Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 1932-6203 | |
dc.identifier.uri | http://hdl.handle.net/11250/2469910 | |
dc.language.iso | eng | nb_NO |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/deed.no | * |
dc.title | Single primer isothermal amplification (SPIA) combined with next generation sequencing provides complete bovine coronavirus genome coverage and higher sequence depth compared to sequence-independent single primer amplification (SISPA) | nb_NO |
dc.type | Journal article | nb_NO |
dc.type | Peer reviewed | nb_NO |
dc.description.version | publishedVersion | nb_NO |
dc.source.journal | PLoS ONE | nb_NO |
dc.identifier.cristin | 1513392 | |
cristin.unitcode | 192,16,2,0 | |
cristin.unitcode | 192,16,3,0 | |
cristin.unitcode | 192,10,1,0 | |
cristin.unitname | Institutt for mattrygghet og infeksjonsbiologi | |
cristin.unitname | Institutt for produksjonsdyrmedisin | |
cristin.unitname | Institutt for husdyr- og akvakulturvitenskap | |
cristin.ispublished | true | |
cristin.fulltext | original | |
cristin.qualitycode | 1 | |