CRISPRMatch: An Automatic Calculation and Visualization Tool for High-throughput CRISPR Genome-editing Data Analysis.

CRISPRMatch: An Automatic Calculation and Visualization Tool for High-throughput CRISPR Genome-editing Data Analysis.
复制标题

CRISPRMatch:用于高通量 CRISPR 基因组编辑数据分析的自动计算和可视化工具

DOI:
10.7150/ijbs.24581
复制
发表时间:
2018
影响因子:
9.2
通讯作者:
Zhang T
Zhang T
中科院分区:
生物学2区
文献类型:
--
作者:
You Q;Zhong Z;Ren Q;Hassan F;Zhang Y;Zhang T

文献摘要

参考文献

被引文献

相似文献

定制设计的核酸酶,包括CRISPR-Cas9和CRISPR-Cpf 1,被广泛用于实现精确的基因组编辑。高通量测序技术的高覆盖率、低成本和可定量性使其成为评价定制核酸酶效率的有效方法。然而,与标准化的转录组协议相比,NGS数据缺乏连接不同工具的用户友好的管道,这些工具可以自动计算突变,评估编辑效率并实现更全面的数据集,可以可视化。在这里,我们开发了一个基于python脚本的自动独立工具包,即CRISPRMatch,通过整合分析步骤,如定位读数和标准化读数计数,计算突变频率(缺失和插入),评估基因组编辑的效率和准确性,以及可视化结果(表格和图形),来处理CRISPR核酸酶转化原生质体的高通量基因组编辑数据。CRISPR-Cas9和CRISPR-Cpf 1核酸酶都得到了CRISPRMatch工具包的支持,集成代码已经在GitHub上发布(https://github.com/zhangtaolab/CRISPRMatch)。
Custom-designed nucleases, including CRISPR-Cas9 and CRISPR-Cpf1, are widely used to realize the precise genome editing. The high-coverage, low-cost and quantifiability make high-throughput sequencing (NGS) to be an effective method to assess the efficiency of custom-designed nucleases. However, contrast to standardized transcriptome protocol, the NGS data lacks a user-friendly pipeline connecting different tools that can automatically calculate mutation, evaluate editing efficiency and realize in a more comprehensive dataset that can be visualized. Here, we have developed an automatic stand-alone toolkit based on python script, namely CRISPRMatch, to process the high-throughput genome-editing data of CRISPR nuclease transformed protoplasts by integrating analysis steps like mapping reads and normalizing reads count, calculating mutation frequency (deletion and insertion), evaluating efficiency and accuracy of genome-editing, and visualizing the results (tables and figures). Both of CRISPR-Cas9 and CRISPR-Cpf1 nucleases are supported by CRISPRMatch toolkit and the integrated code has been released on GitHub (https://github.com/zhangtaolab/CRISPRMatch).
DOI: 10.1016/j.cell.2015.09.038
发表时间: 2015-10-22
期刊: Cell
影响因子: 64.5
作者:
Zetsche B;Gootenberg JS;Abudayyeh OO;Slaymaker IM;Makarova KS;Essletzbichler P;Volz SE;Joung J;van der Oost J;Regev A;Koonin EV;Zhang F
通讯作者: Zhang F
用于多重植物基因组编辑和转录调控的 CRISPR/Cas9 工具箱
DOI: 10.1104/pp.15.00636
发表时间: 2015-10-01
期刊: PLANT PHYSIOLOGY
影响因子: 7.4
作者:
Lowder, Levi G.;Zhang, Dengwei;Qi, Yiping
通讯作者: Qi, Yiping
基于 CRISPR-Cas9 的基因组编辑揭示了水稻 MicroRNA 功能和调控的新见解
DOI: 10.3389/fpls.2017.01598
发表时间: 2017
影响因子: 5.6
作者:
Zhou J;Deng K;Cheng Y;Zhong Z;Tian L;Tang X;Tang A;Zheng X;Zhang T;Qi Y;Zhang Y
通讯作者: Zhang Y
DOI: 10.13345/j.cjb.170171
发表时间: 2017-10-25
期刊: Sheng wu gong cheng xue bao = Chinese journal of biotechnology
影响因子: --
作者:
Li, Hong;Xie, Kabin
通讯作者: Xie, Kabin
DOI: 10.1104/pp.112.205179
发表时间: 2013-01-01
期刊: PLANT PHYSIOLOGY
影响因子: 7.4
作者:
Zhang, Yong;Zhang, Feng;Voytas, Daniel F.
通讯作者: Voytas, Daniel F.