Protocol for high-precision CRISPR-Cas12a-based SNV detection on synthetic DNA, cell line cfDNA models, and liquid biopsies.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2025-06-20 Epub Date: 2025-03-14 DOI:10.1016/j.xpro.2025.103696
Kavish A V Kohabir, Jasper Linthorst, Rob M F Wolthuis, Erik A Sistermans
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Abstract

CRISPR-based diagnostics (CRISPRdx) offer promising tools for rapid and cost-effective genetic testing, but achieving single-nucleotide fidelity remains a challenge. Here, we present a protocol for high-precision detection of single-nucleotide variants (SNVs) using a Cas12a-based approach. We describe how to apply our publicly available ARTEMIS algorithm to identify targetable SNVs, design optimized CRISPR RNAs (crRNAs), and perform fluorescence-based CRISPRdx assays on synthetic DNA, cell line-derived cell-free DNA (cfDNA), and liquid biopsy samples. For complete details on the use and execution of this protocol, please refer to Kohabir et al.1.

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基于crispr - cas12的合成DNA、细胞系cfDNA模型和液体活检的高精度SNV检测方案
基于crispr的诊断(CRISPRdx)为快速和经济有效的基因检测提供了有前途的工具,但是实现单核苷酸保真度仍然是一个挑战。在这里,我们提出了一种使用基于cas12的方法高精度检测单核苷酸变异(snv)的方案。我们描述了如何应用我们公开的ARTEMIS算法来识别可靶向的snv,设计优化的CRISPR rna (crrna),并对合成DNA、细胞系衍生的无细胞DNA (cfDNA)和液体活检样本进行基于荧光的CRISPRdx检测。有关本协议使用和执行的完整细节,请参见Kohabir等人1。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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