Deep learning enhancing guide RNA design for CRISPR/Cas12a‐based diagnostics

Author:

Huang Baicheng1,Guo Ling1,Yin Hang1,Wu Yue1,Zeng Zihan1,Xu Sujie1,Lou Yufeng234,Ai Zhimin1,Zhang Weiqiang1,Kan Xingchi1,Yu Qian1,Du Shimin1,Li Chao56,Wu Lina7,Huang Xingxu1,Wang Shengqi8,Wang Xinjie9ORCID

Affiliation:

1. Zhejiang Lab Hangzhou China

2. Department of Laboratory Medicine, The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou China

3. Key Laboratory of Clinical In Vitro Diagnostic Techniques of Zhejiang Province Hangzhou China

4. Institute of Laboratory Medicine Zhejiang University Hangzhou China

5. Department of Applied Mathematics and Theoretical Physics University of Cambridge Cambridge UK

6. School of Medicine, School of Science and Engineering University of Dundee, Nethergate Dundee UK

7. School of Food Science and Pharmaceutical Engineering Nanjing Normal University Nanjing China

8. Bioinformatics Center of AMMS Beijing China

9. Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen Chinese Academy of Agricultural Sciences Shenzhen China

Abstract

AbstractRapid 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.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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