Evidence map›Paper›PMID 41586153›Full record

ArticleJournal of biomedical optics2026

Artificial-intelligence-driven segmentation and analysis of microbial cells.

Shuang Zhang, Carleton Coffin, Karyn L Rogers, Catherine Ann Royer, Ge Wang

Abstract read
In one paragraph

Article in Journal of biomedical optics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

5 authors.

Shuang ZhangRensselaer Polytechnic Institute, Department of Biomedical Engineering, Troy, New York, United States.ORCID https://orcid.org/0000-0002-5771-5707
Carleton CoffinRensselaer Polytechnic Institute, Department of Biological Sciences, Troy, New York, United States.
Karyn L RogersRensselaer Polytechnic Institute, Department of Earth and Environmental Sciences, Troy, New York, United States.
Catherine Ann RoyerRensselaer Polytechnic Institute, Department of Biological Sciences, Troy, New York, United States.ORCID https://orcid.org/0000-0002-2670-3391
Ge WangRensselaer Polytechnic Institute, Department of Biomedical Engineering, Troy, New York, United States.ORCID https://orcid.org/0000-0002-2656-7705

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significance: Understanding microbial growth and morphology at the single-cell level is essential for studying microbial physiology, providing valuable insights for research and biotechnology. However, existing workflows often rely on manual cell annotation, which limits efficiency and scalability. Therefore, developing an automated workflow for quantitative analysis of cell growth and morphology is highly desirable. Aim: We aim to develop an AI-driven analysis system that efficiently segments and indexes microbial cells, and quantitatively analyzes individual cellular features without requiring expensive annotations, for automated monitoring of cell counts and morphological characteristics. Approach: The automated system consists of four modular components: denoising, zero-shot segmentation using the Segment Anything Model (SAM), structured post-processing, and a quantitative feature extraction. To evaluate the effectiveness of each component, we conducted ablation experiments and systematically studied their impact on the overall system performance. Results: Denoising and post-processing improved segmentation accuracy by 12.10% and 2.30%, respectively. Among the evaluated SAM variants, the SAM-H model achieved the best performance, with an average error rate of only 3.0% across 1162 manually annotated Conclusions: This framework automates quantitative analysis of microbial cells in high-resolution microscopy images. It will enable advanced research on microbial adaptations, with the potential to accelerate studies of extremophiles under harsh environments.

Indexed as

Artificial IntelligenceEscherichia coliImage Processing, Computer-AssistedSingle-Cell AnalysisAlgorithmsIntelligent Systemscell segmentationmicrobial morphologyquantitative cell analysis

Identifiers

PMID41586153
PMCPMC12831121

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Registered trials

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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 OpenQuestion graph.