Department of Chemical and Biomolecular Engineering and University of Tennessee, Knoxville, Tennessee, USA.
Department of Electrical Engineering and Computer Science, University of Tennessee, Knoxville, Tennessee, USA.
CRISPR J. 2022 Aug;5(4):609-617. doi: 10.1089/crispr.2022.0025. Epub 2022 Jul 12.
Both academic and enterprise software solutions exist for designing CRISPR targets. They offer advantages when designing guide RNAs (gRNAs) but often focus on a select number of model organisms. Those that offer a wide variety of organisms can be limited in support of alternative endonucleases and downstream analyses such as multitargeting and population analyses to interrogate a microbiome. To accommodate broad CRISPR utilization, we developed a flexible platform software RISPR ssociated oftware for athway ngineering and esearch (CASPER) for gRNA generation and analysis in any organism and with any CRISPR-Cas system. CASPER combines traditional gRNA design tools with unique functions such as multiple Cas-type gRNA generation and evaluation of spacer redundancy in a single species or microbiome. The analyses have implications for strain-, species-, or genus-specific CRISPR diagnostic probe design and microbiome manipulation. The novel features of CASPER are packaged in a user-friendly interface to create a computational environment for researchers to streamline the utility of CRISPR-Cas systems.
有学术和企业软件解决方案可用于设计 CRISPR 靶点。它们在设计指导 RNA (gRNA) 时有优势,但通常侧重于少数几种模式生物。那些提供多种生物体的方案在支持替代内切酶和下游分析(如多靶点和群体分析以研究微生物组)方面可能受到限制。为了适应广泛的 CRISPR 利用,我们开发了一个灵活的平台软件 RISPR ssociated oftware for athway ngineering and esearch (CASPER),用于在任何生物体中和任何 CRISPR-Cas 系统中生成和分析 gRNA。CASPER 将传统的 gRNA 设计工具与独特的功能结合在一起,例如在单个物种或微生物组中生成多种 Cas 型 gRNA 并评估间隔区冗余。这些分析对于菌株、物种或属特异性的 CRISPR 诊断探针设计和微生物组操作具有重要意义。CASPER 的新颖功能被打包在一个用户友好的界面中,为研究人员创建了一个计算环境,以简化 CRISPR-Cas 系统的实用程序。