Evidence map›Paper›PMID 36214344›Full record

ArticleLab on a chip2022

Deep learning detector for high precision monitoring of cell encapsulation statistics in microfluidic droplets.

Karl Gardner, Md Mezbah Uddin, Linh Tran, Thanh Pham, Siva Vanapalli, Wei Li

Abstract read
In one paragraph

Article in Lab on a chip, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  9. Deep Learning-Assisted Label-Free Parallel Cell Sorting with Digital Microfluidics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
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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

6 authors.

Karl GardnerDepartment of Chemical Engineering, Texas Tech University, 807 Canton Ave, Lubbock, Texas, USA. siva.vanapalli@ttu.edu.
Md Mezbah UddinDepartment of Chemical Engineering, Texas Tech University, 807 Canton Ave, Lubbock, Texas, USA. siva.vanapalli@ttu.edu.
Linh TranDepartment of Chemical Engineering, Texas Tech University, 807 Canton Ave, Lubbock, Texas, USA. siva.vanapalli@ttu.edu.
Thanh PhamDepartment of Chemical Engineering, Texas Tech University, 807 Canton Ave, Lubbock, Texas, USA. siva.vanapalli@ttu.edu.ORCID 0000-0002-6637-9776
Siva VanapalliDepartment of Chemical Engineering, Texas Tech University, 807 Canton Ave, Lubbock, Texas, USA. siva.vanapalli@ttu.edu.
Wei LiDepartment of Chemical Engineering, Texas Tech University, 807 Canton Ave, Lubbock, Texas, USA. siva.vanapalli@ttu.edu.ORCID 0000-0002-4738-1475

Funding

IMAT-ITCR Collaboration: Develop deep learning-based methods to identify subtypes of circulating tumor cells from optical microscope imagesR21CA240185 · NCI · TEXAS TECH UNIVERSITY · PI LI, WEI · 2020 to 2022
$625k
NCI NIH HHS R21 CA240185
6 · The paper itself

Abstract

Encapsulation of cells inside microfluidic droplets is central to several applications involving cellular analysis. Although, theoretically the encapsulation statistics are expected to follow a Poisson distribution, experimentally this may not be achieved due to lack of full control of the experimental variables and conditions. Therefore, there is a need for automatic detection of droplets and cell count enumeration within droplets so a process control feedback to adjust experimental conditions can be implemented. In this study, we use a deep learning object detector called You Only Look Once (YOLO), an influential class of object detectors with several benefits over traditional methods. This paper investigates the application of both YOLOv3 and YOLOv5 object detectors in the development of an automated droplet and cell detector. Experimental data was obtained from a microfluidic flow focusing device with a dispersed phase of cancer cells. The microfluidic device contained an expansion chamber downstream of the droplet generator, allowing for visualization and recording of cell-encapsulated droplet images. In the procedure, a droplet bounding box is predicted, then cropped from the original image for the individual cells to be detected through a separate model for further examination. The system includes a production set for additional performance analysis with Poisson statistics while providing an experimental workflow with both droplet and cell models. The training set is collected and preprocessed before labeling and applying image augmentations, allowing for a generalizable object detector. Precision and recall were utilized as a validation and test set metric, resulting in a high mean average precision (mAP) metric for an accurate droplet detector. To examine model limitations, the predictions were compared to ground truth labels, illustrating that the YOLO predictions closely matched with the droplet and cell labels. Furthermore, it is demonstrated that droplet enumeration from the YOLOv5 model is consistent with hand counted ratios and the Poisson distribution, confirming that the platform can be used in real-time experiments for cell encapsulation optimization.

Indexed as

Deep LearningMicrofluidic Analytical TechniquesCell EncapsulationLab-On-A-Chip DevicesMicrofluidics

Identifiers

PMID36214344
PMCPMC9706597

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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.