# BFS-Net: Weakly Supervised Cell Instance Segmentation from Bright-Field Microscopy Z-Stacks

arXiv: https://arxiv.org/abs/2206.04558 · HTML: https://mlsanity.com/paper/2206.04558/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 9 of its 24 references that are in the map.
- First posted on arXiv 9 Jun 2022.

## Builds on (most cited first, 9 of 9)

- [U-Net: Convolutional Networks for Biomedical Image Segmentation](https://mlsanity.com/paper/1505.04597/) (2015)
- [Mask R-CNN](https://mlsanity.com/paper/1703.06870/) (2017)
- [Grad-CAM: Visual Explanations from Deep Networks via Gradient-based Localization](https://mlsanity.com/paper/1610.02391/) (2016)
- [V-Net: Fully Convolutional Neural Networks for Volumetric Medical Image Segmentation](https://mlsanity.com/paper/1606.04797/) (2016)
- [3D U-Net: Learning Dense Volumetric Segmentation from Sparse Annotation](https://mlsanity.com/paper/1606.06650/) (2016)
- [Weakly Supervised Instance Segmentation using Class Peak Response](https://mlsanity.com/paper/1804.00880/) (2018)
- [PseudoEdgeNet: Nuclei Segmentation only with Point Annotations](https://mlsanity.com/paper/1906.02924/) (2019)
- [Weakly Supervised Cell Instance Segmentation by Propagating from Detection Response](https://mlsanity.com/paper/1911.13077/) (2019)
- [Deep Learning Based Instance Segmentation in 3D Biomedical Images Using Weak Annotation](https://mlsanity.com/paper/1806.11137/) (2018)

## 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.