Evidence map›Paper›PMID 40408631›Full record

ArticlePLoS computational biology2025

Cell-TRACTR: A transformer-based model for end-to-end segmentation and tracking of cells.

Owen M O'Connor, Mary J Dunlop

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Bayesian Transformers and Higher-Order Graph Matching for Cell Tracking in Serial Tissue Sections.Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention · 2026
    Article
  7. Artificial Neural Networks for Bioimage Analysis.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  8. Tui: A Multigenerational and Expert-Correctable Tracker for Cellular Dynamics.Computational and structural biotechnology journal · 2026
    Article
  9. Article
  10. Review
  11. Article
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Owen M O'ConnorBiomedical Engineering, Boston University, Boston, Massachusetts, United States of America.ORCID 0000-0002-6276-6269
Mary J DunlopBiomedical Engineering, Boston University, Boston, Massachusetts, United States of America.ORCID 0000-0002-9261-8216

Funding

National Science Foundation MCB-2032357National Science Foundation MCB-2143289
6 · The paper itself

Abstract

Deep learning-based methods for identifying and tracking cells within microscopy images have revolutionized the speed and throughput of data analysis. These methods for analyzing biological and medical data have capitalized on advances from the broader computer vision field. However, cell tracking can present unique challenges, with frequent cell division events and the need to track many objects with similar visual appearances complicating analysis. Existing architectures developed for cell tracking based on convolutional neural networks (CNNs) have tended to fall short in managing the spatial and global contextual dependencies that are crucial for tracking cells. To overcome these limitations, we introduce Cell-TRACTR (Transformer with Attention for Cell Tracking and Recognition), a novel deep learning model that uses a transformer-based architecture. Cell-TRACTR operates in an end-to-end manner, simultaneously segmenting and tracking cells without the need for post-processing. Alongside this model, we introduce the Cell-HOTA metric, an extension of the Higher Order Tracking Accuracy (HOTA) metric that we adapted to assess cell division. Cell-HOTA differs from standard cell tracking metrics by offering a balanced and easily interpretable assessment of detection, association, and division accuracy. We test our Cell-TRACTR model on datasets of bacteria growing within a defined microfluidic geometry and mammalian cells growing freely in two dimensions. Our results demonstrate that Cell-TRACTR exhibits strong performance in tracking and division accuracy compared to state-of-the-art algorithms, while also meeting traditional benchmarks in detection accuracy. This work establishes a new framework for employing transformer-based models in cell segmentation and tracking.

Indexed as

Cell TrackingImage Processing, Computer-AssistedAlgorithmsCell DivisionComputational BiologyDeep LearningHumansMicroscopyNeural Networks, Computer

Identifiers

PMID40408631
PMCPMC12101859

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.