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A Machine Learning Assisted Label-free Non-invasive Approach for Somatic Reprogramming in Induced Pluripotent Stem Cell Colony Formation Detection and Prediction

机译:机器学习辅助的无标签非侵入性方法用于诱导多能干细胞集落形成检测和预测的体细胞重编程。

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摘要

During cellular reprogramming, the mesenchymal-to-epithelial transition is accompanied by changes in morphology, which occur prior to iPSC colony formation. The current approach for detecting morphological changes associated with reprogramming purely relies on human experiences, which involve intensive amounts of upfront training, human error with limited quality control and batch-to-batch variations. Here, we report a time-lapse-based bright-field imaging analysis system that allows us to implement a label-free, non-invasive approach to measure morphological dynamics. To automatically analyse and determine iPSC colony formation, a machine learning-based classification, segmentation, and statistical modelling system was developed to guide colony selection. The system can detect and monitor the earliest cellular texture changes after the induction of reprogramming in human somatic cells on day 7 from the 20–24 day process. Moreover, after determining the reprogramming process and iPSC colony formation quantitatively, a mathematical model was developed to statistically predict the best iPSC selection phase independent of any other resources. All the computational detection and prediction experiments were evaluated using a validation dataset, and biological verification was performed. These algorithm-detected colonies show no significant differences (Pearson Coefficient) in terms of their biological features compared to the manually processed colonies using standard molecular approaches.
机译:在细胞重编程期间,间充质到上皮的转变伴随着形态的变化,这发生在iPSC集落形成之前。当前用于检测与重新编程相关的形态变化的方法完全依赖于人类经验,其中包括大量的前期培训,有限的质量控制和批次间差异的人为错误。在这里,我们报告一个基于时间流逝的明场成像分析系统,该系统使我们能够实施无标签,无创的方法来测量形态动力学。为了自动分析和确定iPSC菌落的形成,开发了一种基于机器学习的分类,分割和统计建模系统来指导菌落的选择。该系统可以在20至24天的过程的第7天检测到人类体细胞中的重编程后,检测并监测最早的细胞质地变化。此外,在定量确定重编程过程和iPSC集落形成后,开发了一个数学模型,以统计方式预测独立于任何其他资源的最佳iPSC选择阶段。使用验证数据集对所有计算检测和预测实验进行评估,并进行生物学验证。与使用标准分子方法手动处理的菌落相比,这些算法检测到的菌落在生物学特征方面无明显差异(皮尔逊系数)。

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