Evidence map›Paper›PMID 41593031›Full record

ArticleAnalytical chemistry2026

A Facile Method Based on Faster R-CNN for Cell Detection in Microfluidic Devices.

Guillaume Aubry, Yanjun Zhao, Erin Shappell, Jacob M Wheelock, Hang Lu

Abstract read
In one paragraph

Article in Analytical chemistry, 2026. 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

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.

Guillaume AubrySchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive NW, Atlanta, Georgia 30332, United States.ORCID 0000-0001-7828-8508
Yanjun ZhaoCollege of Arts and Sciences, Troy University, Troy, Alabama 36082, United States.
Erin ShappellInterdisciplinary Program in Bioengineering, Georgia Institute of Technology, 311 Ferst Drive NW, Atlanta, Georgia 30332, United States.
Jacob M WheelockInterdisciplinary Program in Bioengineering, Georgia Institute of Technology, 311 Ferst Drive NW, Atlanta, Georgia 30332, United States.
Hang LuSchool of Chemical & Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive NW, Atlanta, Georgia 30332, United States.ORCID 0000-0002-6881-660X

Funding

Inferring multi-scale dynamics underlying behavior in aging C. elegansR01AG082039 · NIA · GEORGIA INSTITUTE OF TECHNOLOGY · PI Gordon Joseph Berman, Hang Lu · 2023 to 2026
$2.1M
Integrative and Quantitative Biosciences Accelerated Training EnvironmentT32GM142616 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI James C. Gumbart, Peng Qiu · 2021 to 2026
$1.8M
NIA NIH HHS R01 AG082039NIGMS NIH HHS T32 GM142616
6 · The paper itself

Abstract

Cell detection is ubiquitous in the analysis of microfluidic cell assays. In cell biology, immunology, oncology, and toxicology research, studying cellular response starts with identifying the cells on chip. The large amount of data generated in such assays requires automating image analysis. While multitudes of image processing tools exist, the microfluidic channel network and crowded cell environment make it difficult to identify and track cells by conventional image processing techniques. In contrast, machine learning-based techniques may overcome this challenge. Two important challenges in implementing these techniques are that it often requires tedious image labeling and coding expertise. Here, we present a facile method for cell detection in microfluidic arrays using Faster region-based convolutional neural network (R-CNN) that addresses both challenges. First, image labeling is fast and easy, because Faster R-CNN only needs bounding boxes as labels to generate training data. Second, we provide a ready-to-use model and a guide for training a Faster R-CNN model that does not require coding expertise. We demonstrate that Faster R-CNN does not need trade-offs between precision and user-friendliness: we created a model that detects cells with an average precision over 98% using a few hundred annotations, which takes less than half an hour. We show that shapes created by the microfluidic structure alone or its interplay with cells are not misidentified as cells. We show for the first time cell detection using Faster R-CNN in microfluidic chips; we envision that this approach will have a broad use in many on-chip fundamental biology and drug-discovery assays.

Indexed as

Lab-On-A-Chip DevicesMicrofluidic Analytical TechniquesConvolutional Neural NetworksHumansImage Processing, Computer-Assisted

Identifiers

PMID41593031
PMCPMC12903050

What OpenQuestion holds

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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.