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dc.contributor.authorStraume, Anne Hege
dc.contributor.authorKjærner-Semb, Erik Nordtorp
dc.contributor.authorSkaftnesmo, Kai Ove
dc.contributor.authorGuralp, Hilal
dc.contributor.authorLillico, Simon
dc.contributor.authorWargelius, Anna
dc.contributor.authorEdvardsen, Rolf Brudvik
dc.date.accessioned2022-03-02T11:41:19Z
dc.date.available2022-03-02T11:41:19Z
dc.date.created2022-02-10T14:14:57Z
dc.date.issued2021
dc.identifier.citationBMC Genomics. 2021, 22 .en_US
dc.identifier.issn1471-2164
dc.identifier.urihttps://hdl.handle.net/11250/2982435
dc.description.abstractNew breeding technologies (NBT) using CRISPR/Cas9-induced homology directed repair (HDR) has the potential to expedite genetic improvement in aquaculture. The long generation time in Atlantic salmon makes breeding an unattractive solution to obtain homozygous mutants and improving the rates of perfect HDR in founder (F0) fish is thus required. Genome editing can represent small DNA changes down to single nucleotide replacements (SNR). This enables edits such as premature stop codons or single amino acid changes and may be used to obtain fish with traits favorable to aquaculture, e.g. disease resistance. A method for SNR has not yet been demonstrated in salmon.en_US
dc.language.isoengen_US
dc.titleSingle nucleotide replacement in the Atlantic salmon genome using CRISPR/Cas9 and asymmetrical oligonucleotide donorsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber8en_US
dc.source.volume22en_US
dc.source.journalBMC Genomicsen_US
dc.identifier.doi10.1186/s12864-021-07823-8
dc.identifier.cristin2000038
dc.relation.projectNorges forskningsråd: 273879en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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