*Result*: AutoFlow: an interactive Shiny app for supervised and unsupervised flow cytometry analysis.

Title:
AutoFlow: an interactive Shiny app for supervised and unsupervised flow cytometry analysis.
Authors:
Woods FER; Safety Sciences, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Trumpington, Cambridge, CB2 0AA, United Kingdom.; Data Sciences & Quantitative Biology, Discovery Sciences, R&D, AstraZeneca, Trumpington, Cambridge, CB2 0AA, United Kingdom., Leonard E; Integrated Bioanalysis, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Trumpington, Cambridge, CB2 0AA, United Kingdom., Ebbels T; Section of Bioinformatics, Department of Metabolism, Digestion & Reproduction, Imperial College London, London, W12 0NN, United Kingdom., Cairns J; Data Sciences & Quantitative Biology, Discovery Sciences, R&D, AstraZeneca, Trumpington, Cambridge, CB2 0AA, United Kingdom., David R; Safety Sciences, Clinical Pharmacology & Safety Sciences, R&D, AstraZeneca, Trumpington, Cambridge, CB2 0AA, United Kingdom.
Source:
Bioinformatics (Oxford, England) [Bioinformatics] 2026 Feb 28; Vol. 42 (3).
Publication Type:
Journal Article
Language:
English
Journal Info:
Publisher: Oxford University Press Country of Publication: England NLM ID: 9808944 Publication Model: Print Cited Medium: Internet ISSN: 1367-4811 (Electronic) Linking ISSN: 13674803 NLM ISO Abbreviation: Bioinformatics Subsets: MEDLINE
Imprint Name(s):
Original Publication: Oxford : Oxford University Press, c1998-
Grant Information:
AstraZeneca
Entry Date(s):
Date Created: 20260215 Date Completed: 20260309 Latest Revision: 20260311
Update Code:
20260311
PubMed Central ID:
PMC12970595
DOI:
10.1093/bioinformatics/btag078
PMID:
41692956
Database:
MEDLINE

*Further Information*

*Motivation: Flow cytometry (FC) is a widely used technique for analysing cells or particles based on the fluorescence of specific markers. Thresholds for fluorescence are typically set manually, a laborious, subjective process that scales poorly as FC technology advances. Machine learning (ML) methods can address these issues but often require technical expertise many bench scientists do not possess. Thus, accessible, open-source, and cross-domain ML-based FC tools are needed.
Results: We present AutoFlow, an easy-to-use, adaptable R Shiny application for automated flow cytometry (FC) analysis. AutoFlow supports two workflows: supervised and unsupervised learning. The application automates key preprocessing steps including fluorescence compensation, debris exclusion, single-cell identification, viability marker gating, and downstream classification or clustering. Across three datasets, two publicly available (Mosmann and Nilsson Rare) and a novel bone marrow microphysiological system (BM-MPS) dataset, AutoFlow demonstrated robust performance. In the supervised workflow, multiclass classification on BM-MPS achieved 97.2% accuracy under a single-timepoint training and multi-timepoint testing scheme, with high sensitivity and specificity across major lineages. For rare populations, performance was strong: Mosmann Rare (0.03% prevalence) achieved 87.5% sensitivity, and 100% specificity, while Nilsson Rare (0.08% prevalence) achieved 87.9% sensitivity, and 99.9% specificity. The unsupervised workflow accurately grouped cells into biologically meaningful clusters, recovering known populations and identifying additional candidate populations with marker profiles consistent with true biology. AutoFlow offers a fast, reproducible, and scalable solution for FC analysis, enabling high-throughput studies and improving the discovery of rare or unexpected cell types.
Availability and Implementation: The application is available at https://github.com/FERWoods/AutoFlow for download using R. An archived version is available at DOI: 10.5281/zenodo.18235796.
(© The Author(s) 2026. Published by Oxford University Press.)*