Predicting and visualizing features of CRISPR-Cas systems

被引:16
作者
Nethery, Matthew A. [1 ,2 ]
Barrangou, Rodolphe [1 ,2 ]
机构
[1] North Carolina State Univ, Genom Sci Grad Program, Raleigh, NC 27695 USA
[2] North Carolina State Univ, Dept Food Bioproc & Nutr Sci, Raleigh, NC 27695 USA
来源
CRISPR-CAS ENZYMES | 2019年 / 616卷
关键词
ACQUIRED-RESISTANCE; MOLECULAR-BIOLOGY; MECHANISTIC BASIS; RNA; SEQUENCE; DIVERSITY; EVOLUTION; DNA; CLASSIFICATION; TRANSCRIPTION;
D O I
10.1016/bs.mie.2018.10.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pervasive application of CRISPR-Cas systems in genome editing has prompted an increase in both interest and necessity to further elucidate existing systems as well as discover putative novel systems. The ubiquity and power of current computational platforms have made in silico approaches to CRISPR-Cas identification and characterization accessible to a wider audience and increasingly amenable for processing extensive data sets. Here, we describe in silico methods for predicting and visualizing notable of CRISPR-Cas systems, including Cas domain determination, CRISPR array visualization, and inference of the protospacer-adjacent motif. The efficiency of these tools enables rapid exploration of CRISPR-Cas diversity across prokaryotic genomes and supports scalable analysis of large genomic data sets.
引用
收藏
页码:1 / 25
页数:25
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