Evidence map›Paper›PMID 40969071›Full record

ArticleSensors (Basel, Switzerland)2025

A Deep Learning-Based Model Approach for Quantitative Analysis of Cell Chemotaxis in a Microfluidic Chip.

Hongxuan Wu, Fei Zhang, Mingji Wei

Abstract read
In one paragraph

Article in Sensors (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

3 authors.

Hongxuan WuSchool of Electrical and Information Engineering, Jiangsu University, Zhenjiang 212013, China.
Fei ZhangSchool of Electrical and Information Engineering, Jiangsu University, Zhenjiang 212013, China.
Mingji WeiSchool of Electrical and Information Engineering, Jiangsu University, Zhenjiang 212013, China.

Funding

the Natural Science Foundation of Jiangsu Province grant No. BK20240851the Natural Science Research of Jiangsu Higher Education Institutions of China (CN) grant No. 18KJB510008the Priority Academic Program Development of Jiangsu Higher Education Institutions No. PAPD-2018-87
6 · The paper itself

Abstract

The rapid and accurate quantitative analysis of cell chemotaxis, which is essential in biology, medicine, and drug development, enables the evaluation of the directional migration capability of cells and the simulation of in vivo cell chemotaxis. However, traditional methods for studying cell chemotaxis often depend on complex experimental procedures, which are not only time-consuming and labor-intensive but also prone to human error. Recently, the rapid advancement of microfluidic technology and deep learning has provided a new way for evaluation of cell chemotaxis. In this study, a chemotaxis evaluation method based on microfluidics and deep learning is proposed. A microfluidic device was designed to simulate cell chemotaxis, allowing for the controlled assessment of cell chemotaxis by generating chemical gradients within microchannels and shear stress. Concurrently, deep learning technology was introduced to identify the migrated and non-migrated states of cell images, thereby enabling the automatic counting and analysis of chemotactic cells. Compared with traditional manual assays, this method not only reduced time and labor costs but also achieved higher accuracy and reproducibility. This innovative approach, which integrates microfluidics and deep learning, provides a novel perspective and tool for cell chemotaxis research. This method not only offers a fresh perspective on cell migration analysis but also has the potential to significantly advance the field of biomedical research, particularly in biosensor development related to drug discovery and disease diagnosis.

Indexed as

ChemotaxisDeep LearningLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesMicrofluidicsBiosensing TechniquesCell MovementHumanscell chemotaxisdeep learningmicrofluidic chipquantitative analysis

Identifiers

PMID40969071
PMCPMC12158346

What OpenQuestion holds

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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 OpenQuestion graph.