Evidence map›Paper›PMID 40188205›Full record

ArticleScientific reports2025

Scale selection and machine learning based cell segmentation and tracking in time lapse microscopy.

Nagasoujanya Annasamudram, Jian Zhao, Olaitan Oluwadare, Aashish Prashanth, Sokratis Makrogiannis

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Nagasoujanya AnnasamudramDivision of Physics, Engineering, Mathematics and Computer Science, Delaware State University, Dover, 19901, DE, USA.
Jian ZhaoDivision of Physics, Engineering, Mathematics and Computer Science, Delaware State University, Dover, 19901, DE, USA.
Olaitan OluwadareDivision of Physics, Engineering, Mathematics and Computer Science, Delaware State University, Dover, 19901, DE, USA.
Aashish PrashanthDivision of Physics, Engineering, Mathematics and Computer Science, Delaware State University, Dover, 19901, DE, USA.
Sokratis MakrogiannisDivision of Physics, Engineering, Mathematics and Computer Science, Delaware State University, Dover, 19901, DE, USA. smakrogiannis@desu.edu.

Funding

Research Capacity CoreU54MD015959 · NIMHD · DELAWARE STATE UNIVERSITY · PI MELISSA A HARRINGTON · 2022 to 2026
$22.6M
QUANTITATIVE IMAGE ANALYSIS TECHNIQUES FOR STUDIES OF AGING PHENOTYPES AND AGE-RELATED DISEASESSC3GM113754 · NIGMS · DELAWARE STATE UNIVERSITY · PI MAKROGIANNIS, SOKRATIS · 2015 to 2024
$686k
Army Research Office W911NF2010095National Science Foundation 2234871NIGMS NIH HHS SC3 GM113754NIGMS NIH HHS SC3GM113754NIMHD NIH HHS 1U54MD015959-01A1NIMHD NIH HHS U54 MD015959
6 · The paper itself

Abstract

Monitoring and tracking of cell motion is a key component for understanding disease mechanisms and evaluating the effects of treatments. Time-lapse optical microscopy has been commonly employed for studying cell cycle phases. However, usual manual cell tracking is very time consuming and has poor reproducibility. Automated cell tracking techniques are challenged by variability of cell region intensity distributions and resolution limitations. In this work, we introduce a comprehensive cell segmentation and tracking methodology. A key contribution of this work is that it employs multi-scale space-time interest point detection and characterization for automatic scale selection and cell segmentation. Another contribution is the use of a neural network with class prototype balancing for detection of cell regions. This work also offers a structured mathematical framework that uses graphs for track generation and cell event detection. We evaluated cell segmentation, detection, and tracking performance of our method on time-lapse sequences of the Cell Tracking Challenge (CTC). We also compared our technique to top performing techniques from CTC. Performance evaluation results indicate that the proposed methodology is competitive with these techniques, and that it generalizes very well to diverse cell types and sizes, and multiple imaging techniques. The code of our method is publicly available on https://github.com/smakrogi/CSTQ_Pub/ , (release v.3.2).

Indexed as

Cell TrackingImage Processing, Computer-AssistedMachine LearningMicroscopyTime-Lapse ImagingAlgorithmsCell MovementHumansNeural Networks, ComputerReproducibility of ResultsAutomated scale selectionCell trackingNeural netSpatio-temporal featuresTime-lapse series

Identifiers

PMID40188205
PMCPMC11972337

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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.