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유전체교정연구단
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Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches

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dc.contributor.authorKwon, J.-
dc.contributor.authorKim, M.-
dc.contributor.authorHwang, W.-
dc.contributor.authorJo, A.-
dc.contributor.authorHwang, G.-H.-
dc.contributor.authorJung, M.-
dc.contributor.authorKim, U.G.-
dc.contributor.authorCui, G.-
dc.contributor.authorKim, H.-
dc.contributor.authorEom, J.-H.-
dc.contributor.authorHur, J.K.-
dc.contributor.authorLee, J.-
dc.contributor.authorKim, Y.-
dc.contributor.authorJin Soo Kim-
dc.contributor.authorBae, S.-
dc.contributor.authorLee, J.K.-
dc.date.accessioned2023-02-28T22:01:00Z-
dc.date.available2023-02-28T22:01:00Z-
dc.date.created2023-01-27-
dc.date.issued2023-01-
dc.identifier.issn1474-7596-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/13057-
dc.description.abstractWe present a novel genome-wide off-target prediction method named Extru-seq and compare it with cell-based (GUIDE-seq), in vitro (Digenome-seq), and in silico methods using promiscuous guide RNAs with large numbers of valid off-target sites. Extru-seq demonstrates a high validation rate and retention of information about the intracellular environment, both beneficial characteristics of cell-based methods. Extru-seq also shows a low miss rate and could easily be performed in clinically relevant cell types with little optimization, which are major positive features of the in vitro methods. In summary, Extru-seq shows beneficial features of cell-based and in vitro methods. © 2023, The Author(s).-
dc.language영어-
dc.publisherBioMed Central Ltd-
dc.titleExtru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000911951200001-
dc.identifier.scopusid2-s2.0-85146106669-
dc.identifier.rimsid79766-
dc.contributor.affiliatedAuthorJin Soo Kim-
dc.identifier.doi10.1186/s13059-022-02842-4-
dc.identifier.bibliographicCitationGenome Biology, v.24, no.1-
dc.relation.isPartOfGenome Biology-
dc.citation.titleGenome Biology-
dc.citation.volume24-
dc.citation.number1-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.subject.keywordPlusUNBIASED DETECTION-
dc.subject.keywordPlusWEB TOOL-
dc.subject.keywordPlusCRISPR-CAS9-
dc.subject.keywordPlusREARRANGEMENTS-
dc.subject.keywordPlusINTEGRATION-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusCLEAVAGE-
dc.subject.keywordAuthorCell-based-
dc.subject.keywordAuthorCRISPR-
dc.subject.keywordAuthorGenome-wide-
dc.subject.keywordAuthorIn vitro-
dc.subject.keywordAuthorOff-target-
Appears in Collections:
Center for Genome Engineering(유전체 교정 연구단) > 1. Journal Papers (저널논문)
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