In Silico Meets In Vivo: Towarcs Computational CRISPR-Based sgRNA Design

被引:81
作者
Chuai, Guo-hui [1 ]
Wang, Qi-Long [2 ]
Liu, Qi [1 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Sch Life Sci & Technol, Dept Cent Lab, Shanghai, Peoples R China
[2] Nanjing Med Univ, Huaian Peoples Hosp 1, Dept Clin Oncol, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
OFF-TARGET CLEAVAGE; GUIDE-RNA DESIGN; WEB TOOL; GENETIC SCREENS; HUMAN-CELLS; GENOME; CAS9; NUCLEASES; ENDONUCLEASE; ENABLES;
D O I
10.1016/j.tibtech.2016.06.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
CRISPR-based genome editing has been widely implemented in various cell types. In silica single guide RNA (sgRNA) design is a key step for successful gene editing using the CRISPR system, and continuing efforts are aimed at refining in silica sgRNA design with high on-target efficacy and reduced off-target effects. Many sgRNA design tools are available, but careful assessments of their application scenarios and performance benchmarks across different types of genome-editing data are needed. Efficient in silico models can be built that integrate current heterogeneous genome-editing data to derive unbiased sgRNA design rules and identify key features for improving sgRNA design. Comprehensive evaluation of on-target and off-target effects of sgRNA will allow more precise genome editing and gene therapies using the CRISPR system.
引用
收藏
页码:12 / 21
页数:10
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