基因组编辑
引导RNA
选择(遗传算法)
清脆的
计算机科学
计算生物学
Cas9
基因
人工智能
生物
遗传学
作者
Jianbo Li,Panfeng Wu,Z. H. Cao,G. S. Huang,Zhike Lu,Jianfeng Yan,Heng Zhang,Yangfan Zhou,Rong Liu,Hui Chen,Lijia Ma,Mengcheng Luo
出处
期刊:Cell Reports
[Elsevier]
日期:2024-02-01
卷期号:43 (2): 113765-113765
标识
DOI:10.1016/j.celrep.2024.113765
摘要
The increasing emergence of Cas9 variants has attracted broad interest, as these variants were designed to expand CRISPR applications. New Cas9 variants typically feature higher editing efficiency, improved editing specificity, or alternative PAM sequences. To select Cas9 variants and gRNAs for high-fidelity and efficient genome editing, it is crucial to systematically quantify the editing performances of gRNAs and develop prediction models based on high-quality datasets. Using synthetic gRNA-target paired libraries and next-generation sequencing, we compared the activity and specificity of gRNAs of four SpCas9 variants. The nucleotide composition in the PAM-distal region had more influence on the editing efficiency of HiFi Cas9 and LZ3 Cas9. We further developed machine learning models to predict the gRNA efficiency and specificity for the four Cas9 variants. To aid users from broad research areas, the machine learning models for the predictions of gRNA editing efficiency within human genome sites are available on our website.
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