Protocol for live cell image segmentation to profile cellular morphodynamics using MARS-Net
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Updated: Sep 7, 2025

Co-culture of Glioblastoma Stem-like Cells on Patterned Neurons to Study Migration and Cellular Interactions
Published on: February 24, 2021
Junbong Jang1, Caleb Hallinan1, Kwonmoo Lee2
1Vascular Biology Program, Boston Children's Hospital, Boston, MA 02115, USA.
Abstract:
Quantitative studies of cellular morphodynamics rely on accurate cell segmentation in live cell images. However, fluorescence and phase contrast imaging hinder accurate edge localization. To address this challenge, we developed MARS-Net, a deep learning model integrating ImageNet-pretrained VGG19 encoder and U-Net decoder trained on the datasets from multiple types of microscopy images. Here, we provide the protocol for installing MARS-Net, labeling images, training MARS-Net for edge localization, evaluating the trained models' performance, and performing the quantitative profiling of cellular morphodynamics. For complete details on the use and execution of this protocol, please refer to Jang et al. (2021).

