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Cas-Database: web-based genome-wide guide RNA library design for gene knockout screens using CRISPR-Cas9

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dc.contributor.authorPark, Jeongbin-
dc.contributor.authorKim, Jin-Soo-
dc.contributor.authorBae, Sangsu-
dc.date.accessioned2020-04-27T12:46:41Z-
dc.date.available2020-04-27T12:46:41Z-
dc.date.created2018-09-19-
dc.date.created2018-09-19-
dc.date.issued2016-07-
dc.identifier.citationBioinformatics, Vol.32 No.13, pp.2017-2023-
dc.identifier.issn1367-4803-
dc.identifier.other55359-
dc.identifier.urihttps://hdl.handle.net/10371/165662-
dc.description.abstractMotivation: CRISPR-derived RNA guided endonucleases (RGENs) have been widely used for both gene knockout and knock-in at the level of single or multiple genes. RGENs are now available for forward genetic screens at genome scale, but single guide RNA (sgRNA) selection at this scale is difficult. Results: We develop an online tool, Cas-Database, a genome-wide gRNA library design tool for Cas9 nucleases from Streptococcus pyogenes (SpCas9). With an easy-to-use web interface, Cas-Database allows users to select optimal target sequences simply by changing the filtering conditions. Furthermore, it provides a powerful way to select multiple optimal target sequences from thousands of genes at once for the creation of a genome-wide library. Cas-Database also provides a web application programming interface (web API) for advanced bioinformatics users.-
dc.language영어-
dc.publisherOxford University Press-
dc.titleCas-Database: web-based genome-wide guide RNA library design for gene knockout screens using CRISPR-Cas9-
dc.typeArticle-
dc.contributor.AlternativeAuthor김진수-
dc.identifier.doi10.1093/bioinformatics/btw103-
dc.citation.journaltitleBioinformatics-
dc.identifier.wosid000379761500013-
dc.identifier.scopusid2-s2.0-85007179516-
dc.citation.endpage2023-
dc.citation.number13-
dc.citation.startpage2017-
dc.citation.volume32-
dc.identifier.sci000379761500013-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Jin-Soo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusOFF-TARGET SITES-
dc.subject.keywordPlusHUMAN-CELLS-
dc.subject.keywordPlusFUNCTIONAL GENOMICS-
dc.subject.keywordPlusTOOL-
dc.subject.keywordPlusSYSTEM-
dc.subject.keywordPlusCRISPR/CAS9-
dc.subject.keywordPlusNUCLEASES-
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  • College of Natural Sciences
  • Department of Chemistry
Research Area Biology and Biochemistry

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