“…A variety of signal processing techniques, including support vector machine (SVM), intensity histogram and intensity surface curvature, level-set segmentation, and k-nearest neighbor, have been applied to fluorescence intensity images to perform classification. In recent years, with the rapid development of parallel-computing capability and deep learning algorithms, convolutional neural networks have also been applied to fluorescence images of single cells for cell cycle tracking. , Since all these methods are based on fluorescence microscopy, they inevitably face the associated limitations, including photobleaching, chemical, and phototoxicity, weak fluorescent signals that require large exposures, as well as nonspecific binding. These constraints limit the applicability of fluorescence imaging to studying live cell cultures over large temporal scales …”