清脆的
基因组编辑
Cas9
计算生物学
基因组
生物
基因座(遗传学)
引导RNA
基因
遗传学
计算机科学
作者
Claude Van Campenhout,Pauline Cabochette,Anne-Clémence Veillard,Miklós Laczik,Agnieszka Zelisko-Schmidt,Céline Sabatel,Maxime Dhainaut,Benoît Vanhollebeke,Cyril Gueydan,Véronique Kruys
出处
期刊:BioTechniques
[Future Science Ltd]
日期:2019-05-01
卷期号:66 (6): 295-302
被引量:38
标识
DOI:10.2144/btn-2018-0187
摘要
CRISPR/Cas9 technology has evolved as the most powerful approach to generate genetic models both for fundamental and preclinical research. Despite its apparent simplicity, the outcome of a genome-editing experiment can be substantially impacted by technical parameters and biological considerations. Here, we present guidelines and tools to optimize CRISPR/Cas9 genome-targeting efficiency and specificity. The nature of the target locus, the design of the single guide RNA and the choice of the delivery method should all be carefully considered prior to a genome-editing experiment. Different methods can also be used to detect off-target cleavages and decrease the risk of unwanted mutations. Together, these optimized tools and proper controls are essential to the assessment of CRISPR/Cas9 genome-editing experiments.
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