Aug 2026· Medical Image Analysis· Vol 114, pp.
104275
· 0 citations· 68 references
Medicine
TL;DR
This work proposes a unified framework based on Graph Neural Networks for simultaneous bacteria tracking, division detection, and life cycle state classification and introduces a network-based approach for segmentation error correction using division and multi-frame correspondence predictions.
Abstract
For understanding dynamic biological processes such as the life cycle progression of bacteria at the single-cell level, automatic methods for tracking and state classification are needed. In this work, we propose a unified framework based on Graph Neural Networks for simultaneous bacteria tracking, division detection, and life cycle state classification. In previous work, these tasks were treated separately. With our method, trajectories are represented by a graph, where nodes represent bacteria at different time points of a live-cell microscopy video, and edges represent their interactions over multiple frames. Tracking, division detection, and life cycle state classification are performed simultaneously by classifying graph nodes and edges. For all three tasks, we use visual object features from a large-scale pretrained foundation model. This eliminates the need for separately-trained task-specific CNN encoders as used in previous work and enhances the robustness. In addition, we introduce a network-based approach for segmentation error correction using division and multi-frame correspondence predictions. Our method was evaluated using live-cell bright-field microscopy videos of spore germination and outgrowth of rod-shaped bacteria. Our experiments show that the proposed method outperforms existing methods for division detection and state classification. The method yields state-of-the-art results for bacteria tracking and shows increased robustness against segmentation errors as well as image distortions.
The proposed HOCT is easier to fine-tune, quickly reducing tracking errors by 59% with 400 annotations in a human-in-the-loop setting, outperforming LoRA fine-tuning of competing transformer baselines (6.75% improvement).
Jordão Bragantini, Ilan Theodoro, L. Royer· arXiv.org· 0 citations
The results show that dynamic information, rather than static morphology alone, drives accurate cell-state classification, and that 3D architectures are needed to fully exploit it for label-free dynamic phenotyping.
S. Alizada, Kayla Marks, R. Zitnay et al.· bioRxiv· 0 citations
The results suggest that temporal context is not automatically sufficient to improve early S detection, and more careful temporal model design, training strategy, and evaluation using consistent data splits are needed to determine whether temporal information can improve Hoechst-based cell-cycle segmentation.
Particular attention is given to small-sample fine-tuning and human-in-the-loop workflows, which aim to adapt pretrained segmentation and tracking models to laboratory-specific microscopy data while reducing annotation effort and improving the reliability of downstream biological conclusions.
A step-by-step protocol for automated cell viability quantification from two-channel live/dead fluorescence images using a deep learning pipeline built on a U-Net architecture with a ResNet-50 encoder pretrained on ImageNet, providing a reproducible framework adaptable to diverse cell types and imaging platforms.
Álvaro Díaz Vera, Khan Sharun, S. A. Banu et al.· Methods in molecular biology· 0 citations
A new unsupervised method for cell instance segmentation and phenotypic classification from unlabeled microscopy images is described, based on reconstructing each image using a coarse-to-fine routing pyramid that associates pixels with spatially sparse latent sources.
Zi-Wen Liu, Martin Weigert· 0 citations
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