Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity.
摘要:
The RNA-guided Cas9 nuclease can tolerate certain mismatches to the DNA target and can thereby promote undesired off-target mutagenesis. A "double nicking" strategy has been developed to significantly reduce off-target activity in cell lines and to facilitate efficient gene knockout in mouse zygotes, enabling genome editing applications with higher levels of specificity.
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关键词:
ZINC-FINGER NUCLEASES TAL EFFECTORS HUMAN-CELLS BACTERIA SYSTEM TRANSCRIPTION ENDONUCLEASE GENERATION MUTATIONS KNOCKOUT
DOI:
10.1016/j.cell.2013.08.021
被引量:
年份:
2013





































































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