BFS-Net: Weakly Supervised Cell Instance Segmentation from Bright-Field Microscopy Z-Stacks
Not on the map. Why?
Abstract (arXiv)
Despite its broad availability, volumetric information acquisition from Bright-Field Microscopy (BFM) is inherently difficult due to the projective nature of the acquisition process. We investigate the prediction of 3D cell instances from a set of BFM Z-Stack images. We propose a novel two-stage weakly supervised method for volumetric instance segmentation of cells which only requires approximate cell centroids annotation. Created pseudo-labels are thereby refined with a novel refinement loss with Z-stack guidance. The evaluations show that our approach can generalize not only to BFM Z-Stack data, but to other 3D cell imaging modalities. A comparison of our pipeline against fully supervised methods indicates that the significant gain in reduced data collection and labelling results in minor performance difference.
Key facts. No citing papers in the map yet (data through 7 Oct 2026). Builds on 9 of its 24 references that are in the map. First posted on arXiv 9 Jun 2022.
Builds on
9 of 24 references.
References · 9
- 2015U-Net: Convolutional Networks for Biomedical Image Segmentationcited by 19,604
- 2017Mask R-CNNcited by 7,259
- 2016Grad-CAM: Visual Explanations from Deep Networks via Gradient-based Localizationcited by 6,690
- 2016V-Net: Fully Convolutional Neural Networks for Volumetric Medical Image Segmentationcited by 2,284
- 20163D U-Net: Learning Dense Volumetric Segmentation from Sparse Annotationcited by 1,471
- 2018Weakly Supervised Instance Segmentation using Class Peak Responsecited by 74
- 2019PseudoEdgeNet: Nuclei Segmentation only with Point Annotationscited by 27
- 2019Weakly Supervised Cell Instance Segmentation by Propagating from Detection Responsecited by 17
- 2018Deep Learning Based Instance Segmentation in 3D Biomedical Images Using Weak Annotationcited by 11
Built on by
Not cited yet.