Evidence map›Paper›PMID 41190506›Full record

ReviewLab on a chip2025

Transforming microfluidics for single-cell analysis with robotics and artificial intelligence.

Jinxiong Cheng, Rajiv Anne, Yu-Chih Chen

Abstract readReview
In one paragraph

Review in Lab on a chip, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
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  5. 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.

Jinxiong ChengDepartment of Bioengineering, Swanson School of Engineering, University of Pittsburgh, 3700 O'Hara Street, Pittsburgh, PA 15260, USA.ORCID 0000-0002-0667-8707
Rajiv AnneDepartment of Bioengineering, Swanson School of Engineering, University of Pittsburgh, 3700 O'Hara Street, Pittsburgh, PA 15260, USA.
Yu-Chih ChenDepartment of Bioengineering, Swanson School of Engineering, University of Pittsburgh, 3700 O'Hara Street, Pittsburgh, PA 15260, USA.ORCID 0000-0002-3875-4671

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 1988 to 2026
$158.0M
Project 3: Hedgehog Inhibition to Enhance Response to ICI TherapyP50CA272218 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FRANCESMARY MODUGNO · 2023 to 2026
$11.0M
Deciphering Cellular Heterogeneity and Inheritability in MigrationR35GM150509 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Yu-Chih Chen · 2023 to 2026
$1.5M
Halting Breast Cancer Metastasis by Blocking Cancer-MSC EngulfmentR21CA293424 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Yu-Chih Chen · 2025 to 2026
$398k
NCI NIH HHS P30 CA047904NCI NIH HHS P50 CA272218NCI NIH HHS R21 CA293424NIGMS NIH HHS R35 GM150509
6 · The paper itself

Abstract

Single-cell analysis has advanced biomedical research by revealing cellular heterogeneity with unprecedented resolution, identifying rare subpopulations that drive disease progression and therapeutic resistance. Microfluidics is central to this advancement, enabling precise single-cell isolation, manipulation, and cellular profiling. However, limitations in automation, reliability, and technical barriers hinder the widespread adoption of microfluidic single-cell analysis. This review highlights key innovations in experimental methods and deep learning-driven data analysis to overcome these challenges. Operating microfluidics with robotic operation, digital microfluidics, or microrobots enhances experimental precision and scalability. Beyond experimental automation, deep learning revolutionizes data interpretation through label-free image processing and cell status classification and regression. Generative models further refine analysis by correcting batch effects and generating synthetic datasets, improving accuracy and reproducibility in single-cell studies. Considering the complexity of integrating these technologies, remote shared cloud labs represent a potential pathway toward standardized and high-throughput single-cell analysis, facilitating broader access to advanced experimental workflows. Overall, the convergence of robotics and artificial intelligence in single-cell analysis will change data acquisition, hypothesis testing, and model refinement, driving breakthroughs in drug discovery and personalized medicine. While implementation remains challenging, this paradigm shift is transforming biomedical research, enabling unprecedented precision, scalability, and data-driven innovation.

Indexed as

Artificial IntelligenceMicrofluidic Analytical TechniquesMicrofluidicsRoboticsSingle-Cell AnalysisAnimalsDeep LearningHumansLab-On-A-Chip Devices

Identifiers

PMID41190506
PMCPMC12587405

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.