清脆的
核酸
核酸检测
计算生物学
工作流程
数字聚合酶链反应
计算机科学
纳米技术
微流控
多路复用
回文
翻译(生物学)
数字微流体
化学
高分辨率
蛋白质检测
生物标志物
分辨率(逻辑)
序列(生物学)
生物
DNA
作者
Yang Zhang,Roy S. K. Walker,Anwar Sunna,Tracie Barber,M. Li
标识
DOI:10.1002/advs.202517470
摘要
Droplet digital (dd) clustered regularly interspaced short palindromic repeats (CRISPR) integrates the high sequence specificity of CRISPR-based nucleic acid detection with the absolute quantification capability of digital droplet microfluidics, offering high sensitivity, precision, and scalability. By partitioning samples into thousands to millions of picoliter microdroplets, ddCRISPR enables single-molecule resolution and minimizes background interference. This review summarizes the principles of droplet generation, manipulation, and detection in ddCRISPR platforms, as well as recent advances in amplification-based and amplification-free detection strategies. Representative applications are highlighted for viral, bacterial, and other DNA/RNA biomarker detection. Current challenges, including workflow automation, droplet stability, multiplexing, and assay portability, are discussed alongside future perspectives such as artificial intelligence (AI)-assisted analysis, point-of-care integration, and high-throughput multiplexed detection. These insights aim to guide the translation of ddCRISPR technologies from laboratory research to robust, scalable, and accessible diagnostic solutions.
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