Learning to Segment Dense Cell Nuclei with Shape Prior

Abstract

We study the problem of segmenting multiple cell nuclei from GFP or Hoechst stained microscope images with a shape prior. This problem is encountered ubiquitously in cell biology and developmental biology. Our work is motivated by the observation that segmentations with loose boundary or shrinking bias not only jeopardize feature extraction for downstream tasks (e.g. cell tracking), but also prevent robust statistical analysis (e.g. modeling of fluorescence distribution). We therefore propose a novel extension to the graph cut framework that incorporates a "blob"-like shape prior. The corresponding energy terms are parameterized via structured learning. Extensive evaluation and comparison on 2D/3D datasets show substantial quantitative improvement over other state-of-the-art methods. For example, our method achieves an 8.2% Rand index increase and a 4.3 Hausdorff distance decrease over the second best method on a public hand-labeled 2D benchmark.

Cite

Text

Lou et al. "Learning to Segment Dense Cell Nuclei with Shape Prior." IEEE/CVF Conference on Computer Vision and Pattern Recognition, 2012. doi:10.1109/CVPR.2012.6247778

Markdown

[Lou et al. "Learning to Segment Dense Cell Nuclei with Shape Prior." IEEE/CVF Conference on Computer Vision and Pattern Recognition, 2012.](https://mlanthology.org/cvpr/2012/lou2012cvpr-learning/) doi:10.1109/CVPR.2012.6247778

BibTeX

@inproceedings{lou2012cvpr-learning,
  title     = {{Learning to Segment Dense Cell Nuclei with Shape Prior}},
  author    = {Lou, Xinghua and Köthe, Ullrich and Wittbrodt, Jochen and Hamprecht, Fred A.},
  booktitle = {IEEE/CVF Conference on Computer Vision and Pattern Recognition},
  year      = {2012},
  pages     = {1012-1018},
  doi       = {10.1109/CVPR.2012.6247778},
  url       = {https://mlanthology.org/cvpr/2012/lou2012cvpr-learning/}
}