生物
生物信息学
计算生物学
索引
清脆的
桑格测序
斑马鱼
瓶颈
基因组
遗传学
DNA测序
DNA
基因
计算机科学
单核苷酸多态性
基因型
嵌入式系统
作者
Christelle Etard,Swarnima Joshi,Johannes Stegmaier,Ralf Mikut,Uwe Strähle
出处
期刊:Zebrafish
[Mary Ann Liebert, Inc.]
日期:2017-08-02
卷期号:14 (6): 586-588
被引量:26
标识
DOI:10.1089/zeb.2017.1454
摘要
A bottleneck in CRISPR/Cas9 genome editing is variable efficiencies of in silico-designed gRNAs. We evaluated the sensitivity of the TIDE method (Tracking of Indels by DEcomposition) introduced by Brinkman et al. in 2014 for assessing the cutting efficiencies of gRNAs in zebrafish. We show that this simple method, which involves bulk polymerase chain reaction amplification and Sanger sequencing, is highly effective in tracking well-performing gRNAs in pools of genomic DNA derived from injected embryos. The method is equally effective for tracing INDELs in heterozygotes.
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