利用深度学习进行细胞病理效应检测和克隆选择。

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pharmaceutical Research Pub Date : 2024-08-01 Epub Date: 2024-07-24 DOI:10.1007/s11095-024-03749-4
Yu Yuan, Tony Wang, Jordan Sims, Kim Le, Cenk Undey, Erdal Oruklu
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引用次数: 0

摘要

目的:在生物技术领域,显微细胞成像通常用于识别和分析细胞形态和细胞状态,应用范围广泛。例如,显微镜可用于检测细胞培养样本中是否存在细胞病理效应(CPE),以确定是否受到病毒污染。显微镜的另一个应用是在细胞系开发过程中验证克隆性。传统上,这些显微图像的检测都是由人工分析师手动完成的。这既繁琐又耗时。在本文中,我们建议使用有监督的深度学习算法来自动完成上述细胞检测过程:方法:所提出的算法利用图像处理技术和卷积神经网络(CNN)来检测 CPE 的存在,并验证细胞系开发中的克隆性:我们在由领域专家收集和标注的图像数据上对算法进行了训练和测试。我们的实验在准确性和速度方面都取得了可喜的成果:深度学习算法在 CPE 检测和克隆选择应用中都达到了很高的准确率(超过 95%),从而实现了高效、经济的自动化流程。
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Cytopathic Effect Detection and Clonal Selection using Deep Learning.

Purpose: In biotechnology, microscopic cell imaging is often used to identify and analyze cell morphology and cell state for a variety of applications. For example, microscopy can be used to detect the presence of cytopathic effects (CPE) in cell culture samples to determine virus contamination. Another application of microscopy is to verify clonality during cell line development. Conventionally, inspection of these microscopy images is performed manually by human analysts. This is both tedious and time consuming. In this paper, we propose using supervised deep learning algorithms to automate the cell detection processes mentioned above.

Methods: The proposed algorithms utilize image processing techniques and convolutional neural networks (CNN) to detect the presence of CPE and to verify the clonality in cell line development.

Results: We train and test the algorithms on image data which have been collected and labeled by domain experts. Our experiments have shown promising results in terms of both accuracy and speed.

Conclusion: Deep learning algorithms achieve high accuracy (more than 95%) on both CPE detection and clonal selection applications, resulting in a highly efficient and cost-effective automation process.

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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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