Metagenomic CRISPR Array Analysis Tool: a novel graph-based approach to finding CRISPR arrays in metagenomic datasets.

microLife Pub Date : 2025-07-17 eCollection Date: 2025-01-01 DOI:10.1093/femsml/uqaf016
Fikrat Talibli, Björn Voß
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引用次数: 0

Abstract

Clustered Regularly Interspersed Short Palindromic Repeats and CRISPR-associated genes (CRISPR-Cas) is a bacterial immune system also famous for its use in genome editing. The diversity of known systems could be significantly increased by metagenomic data. Here we present the Metagenomic CRISPR Array Analysis Tool (MCAAT), a highly sensitive algorithm for finding CRISPR arrays in unassembled metagenomic data. It takes advantage of the properties of CRISPR arrays that form multicycles in de Bruijn graphs. We show that MCAAT reliably predicts CRISPR arrays in bacterial genome sequences and that its assembly-free graph-based strategy outperforms assembly-based workflows and other assembly-free methods on synthetic and real metagenomes. Our new approach will help to increase the diversity of known CRISPR-Cas systems and enable studies of spacer evolution within metagenomic data sets.

宏基因组CRISPR阵列分析工具:一种在宏基因组数据集中寻找CRISPR阵列的基于图形的新方法。
聚集规律穿插短回文重复序列和crispr相关基因(CRISPR-Cas)是一种细菌免疫系统,也因其在基因组编辑中的应用而闻名。已知系统的多样性可以通过宏基因组数据显着增加。在这里,我们提出了宏基因组CRISPR阵列分析工具(MCAAT),这是一种高度敏感的算法,用于在未组装的宏基因组数据中寻找CRISPR阵列。它利用了CRISPR阵列在德布鲁因图中形成多周期的特性。我们表明,MCAAT可靠地预测细菌基因组序列中的CRISPR阵列,并且其基于无装配图的策略优于基于装配的工作流程和其他合成和真实宏基因组的无装配方法。我们的新方法将有助于增加已知CRISPR-Cas系统的多样性,并使宏基因组数据集中的间隔进化研究成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
5.50
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0.00%
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