深度学习增强了基于 CRISPR/Cas12a 诊断的引导 RNA 设计

IF 23.7 Q1 MICROBIOLOGY iMeta Pub Date : 2024-06-15 DOI:10.1002/imt2.214
Baicheng Huang, Ling Guo, Hang Yin, Yue Wu, Zihan Zeng, Sujie Xu, Yufeng Lou, Zhimin Ai, Weiqiang Zhang, Xingchi Kan, Qian Yu, Shimin Du, Chao Li, Lina Wu, Xingxu Huang, Shengqi Wang, Xinjie Wang
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摘要

快速准确的诊断检测是改善患者预后和防治传染病的基础。基于簇状正则间隔短回文重复序列(CRISPR)的 Cas12a 检测系统已成为现场核酸检测的一种前景广阔的解决方案。然而,为基于 Cas12a 的检测有效设计 CRISPR RNA(crRNA)仍具有挑战性且耗时较长。在本研究中,我们提出了一种用于 Cas12a 介导的诊断的深度学习增强型 crRNA 设计系统,简称为 EasyDesign。该系统采用了一个优化的卷积神经网络(CNN)预测模型,该模型是在由 11,496 个经实验验证的基于 Cas12a 的检测案例组成的综合数据集上训练的,涵盖了广泛的流行病原体,达到了 Spearman's ρ = 0.812。我们还进一步评估了该模型在针对未纳入训练数据的四种病原体设计 crRNA 时的性能:猴痘病毒、肠病毒 71、柯萨奇病毒 A16 和李斯特菌。结果表明,与传统的实验筛选相比,预测性能更优越。此外,我们还开发了一个交互式网络服务器(https://crispr.zhejianglab.com/),将 EasyDesign 与重组酶聚合酶扩增(RPA)引物设计整合在一起,提高了用户的可访问性。通过这个基于网络的平台,我们成功地为六种人类乳头瘤病毒(HPV)亚型设计出了最佳的 Cas12a crRNA。值得注意的是,在 CRISPR 检测中,每种 HPV 亚型的所有前五名预测 crRNA 都表现出强大的荧光信号,从而表明该平台可有效促进临床样本检测。总之,EasyDesign 为基于 Cas12a 检测的 crRNA 设计提供了快速可靠的解决方案,可作为临床诊断和研究应用的重要工具。
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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Deep learning enhancing guide RNA design for CRISPR/Cas12a-based diagnostics

Rapid and accurate diagnostic tests are fundamental for improving patient outcomes and combating infectious diseases. The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Cas12a-based detection system has emerged as a promising solution for on-site nucleic acid testing. Nonetheless, the effective design of CRISPR RNA (crRNA) for Cas12a-based detection remains challenging and time-consuming. In this study, we propose an enhanced crRNA design system with deep learning for Cas12a-mediated diagnostics, referred to as EasyDesign. This system employs an optimized convolutional neural network (CNN) prediction model, trained on a comprehensive data set comprising 11,496 experimentally validated Cas12a-based detection cases, encompassing a wide spectrum of prevalent pathogens, achieving Spearman's ρ = 0.812. We further assessed the model performance in crRNA design for four pathogens not included in the training data: Monkeypox Virus, Enterovirus 71, Coxsackievirus A16, and Listeria monocytogenes. The results demonstrated superior prediction performance compared to the traditional experiment screening. Furthermore, we have developed an interactive web server (https://crispr.zhejianglab.com/) that integrates EasyDesign with recombinase polymerase amplification (RPA) primer design, enhancing user accessibility. Through this web-based platform, we successfully designed optimal Cas12a crRNAs for six human papillomavirus (HPV) subtypes. Remarkably, all the top five predicted crRNAs for each HPV subtype exhibited robust fluorescent signals in CRISPR assays, thereby suggesting that the platform could effectively facilitate clinical sample testing. In conclusion, EasyDesign offers a rapid and reliable solution for crRNA design in Cas12a-based detection, which could serve as a valuable tool for clinical diagnostics and research applications.

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