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Updated: May 1, 2026

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Published on: February 22, 2016
A rapid and efficient 2D/3D nuclear segmentation method for analysis of early mouse embryo and stem cell image data
Xinghua Lou1, Minjung Kang2, Panagiotis Xenopoulos1
1Developmental Biology Program, Sloan-Kettering Institute, New York, NY 10065, USA.
We developed MINS, a new software tool for accurate cell counting and analysis in microscopic images. This user-friendly tool improves segmentation accuracy for early mouse embryo and stem cell research.
Area of Science:
- Biomedical imaging
- Cell biology
- Image analysis
Background:
- Microscopic image analysis, particularly cell detection, faces challenges with existing commercial software for early mouse embryo and stem cell data.
- Accurate segmentation is crucial for quantitative analysis in cell biology research.
Purpose of the Study:
- To develop a user-friendly, accurate, and efficient software tool for cell counting and fluorescent intensity measurements.
- To address the limitations of current software in analyzing 2D and 3D microscopic images of early mouse embryos and stem cells.
Main Methods:
- Developed MINS (modular interactive nuclear segmentation), a MATLAB/C++ based tool.
- Implemented a three-module pipeline: detection, segmentation, and cell position classification.
- Evaluated MINS on both 2D and 3D image datasets and compared it with existing tools.
Main Results:
- MINS demonstrated improved segmentation accuracy and usability compared to related tools.
- The software is effective for both 2D and 3D image data.
- MINS provides accurate cell counting and fluorescent intensity measurements.
Conclusions:
- MINS offers a significant advancement in microscopic image analysis for cell research.
- Its accuracy and ease of use make it suitable for routine single-cell-level image analyses.
- The tool addresses a critical need in the analysis of early mouse embryo and stem cell images.
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