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Related Concept Videos

Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

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Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
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Related Experiment Video

Updated: Sep 11, 2025

Digital Inline Holographic Microscopy DIHM of Weakly-scattering Subjects
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DL-CSPF: deep-learning-based cell segmentation with a physical framework for digital holographic microscopy.

Zhuoshi Li, Haojie Gu, Linpeng Lu

    Applied Optics
    |August 12, 2025
    PubMed
    Summary
    This summary is machine-generated.

    Accurate live-cell segmentation is vital for research. DL-CSPF, a novel deep-learning method, precisely segments cells from digital holographic microscopy images, enabling reliable quantitative analysis of cellular dynamics.

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    Area of Science:

    • Biomedical Imaging
    • Cell Biology
    • Computational Biology

    Background:

    • Digital holographic microscopy (DHM) provides label-free, quantitative phase imaging of live cells.
    • Accurate cell segmentation is essential for quantitative analysis but challenging due to complex cellular states and imaging conditions.

    Purpose of the Study:

    • To introduce DL-CSPF, a deep-learning-based method for high-precision live-cell segmentation.
    • To address challenges in cell segmentation accuracy for long-term quantitative analysis.

    Main Methods:

    • DL-CSPF employs two neural networks for foreground-background segmentation and cell detection, generating foreground edges and seed points.
    • A marker-controlled watershed algorithm utilizes these features for cell segmentation.
    • The method focuses on low information entropy features, reducing dataset requirements and eliminating manual parameter tuning.

    Main Results:

    • DL-CSPF demonstrated accurate segmentation across diverse datasets (HeLa, pollen, COS-7 cells).
    • Validated feasibility and generalization in various imaging conditions.
    • Reliably characterized and quantitatively analyzed morphological metrics during long-term live-cell imaging.

    Conclusions:

    • DL-CSPF offers a robust and accurate solution for live-cell segmentation using DHM.
    • The method facilitates precise quantitative analysis of cellular morphology throughout the lifecycle.
    • DL-CSPF is a promising tool for advancing biomedical research.