IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0319532.html
   My bibliography  Save this article

SAMCell: Generalized label-free biological cell segmentation with segment anything

Author

Listed:
  • Alexandra Dunnum VandeLoo
  • Nathan J Malta
  • Saahil Sanganeriya
  • Emilio Aponte
  • Caitlin van Zyl
  • Danfei Xu
  • Craig Forest

Abstract

Background: When analyzing cells in culture, assessing cell morphology (shape), confluency (density), and growth patterns are necessary for understanding cell health. These parameters are generally obtained by a skilled biologist inspecting light microscope images, but this can become very laborious for high-throughput applications. One way to speed up this process is by automating cell segmentation. Cell segmentation is the task of drawing a separate boundary around each cell in a microscope image. This task is made difficult by vague cell boundaries and the transparent nature of cells. Many techniques for automatic cell segmentation exist, but these methods often require annotated datasets, model retraining, and associated technical expertise.Results: We present SAMCell, a modified version of Meta’s Segment Anything Model (SAM) trained on an existing large-scale dataset of microscopy images containing varying cell types and confluency. Our approach works on a wide range of microscopy images, including cell types not seen in training and on images taken by a different microscope. We also present a user-friendly UI that reduces the technical expertise needed for this automated microscopy technique.Conclusions: Using SAMCell, biologists can quickly and automatically obtain cell segmentation results of higher quality than previous methods. Further, these results can be obtained through our custom Graphical User Interface, thus decreasing the human labor required in cell culturing.

Suggested Citation

  • Alexandra Dunnum VandeLoo & Nathan J Malta & Saahil Sanganeriya & Emilio Aponte & Caitlin van Zyl & Danfei Xu & Craig Forest, 2025. "SAMCell: Generalized label-free biological cell segmentation with segment anything," PLOS ONE, Public Library of Science, vol. 20(9), pages 1-21, September.
  • Handle: RePEc:plo:pone00:0319532
    DOI: 10.1371/journal.pone.0319532
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0319532
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0319532&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0319532?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0319532. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.