Comparison of Deep-Learning Models for Classification of Cellular Phenotype From Flow Cytometry Data

This study compares the relative utility of deep learning models as automated phenotypic classifiers, built with features of peripheral blood cell populations assayed with flow cytometry. We report surprisingly good sensitively for the task of distinguishing male from female mice solely from attributes of cells present in peripheral blood samples. This novel application of cytometry technology is easily validated and represents an example use that is not reliably possible with current visual analysis techniques. It serves as a useful test case with known ground truth labels of a subtle cellular phenotype and indicates the potential of this approach to more biologically meaningful phenotypes. We evaluate three different deep neural network architectures that vary in how the high-dimensional flow cytometry data is processed as input: 1) a convolutional neural network applied to the raw, per-cell marker intensity values, 2) a multi-layer perceptron taking per-channel histograms representing the range of intensities for a given marker, and 3) a multi-layer perceptron using a hypervoxel representation of the set of marker intensities for each cell in a given input sample. Our results show the histogram-based multi-layer perceptron achieves the highest classification accuracy of 91% on 2300 mouse blood samples for a mutant phenotype classification task. This indicates the value of deep learning models for detection of subtle signals that are not readily observed in high dimensions by visual analysis. These results demonstrate the effectiveness of deep learning for automated analysis of flow cytometry data on a challenging and biologically complex classification task.

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Publication Details

Journal
IEEE Transactions on Computational Biology and Bioinformatics
Published
2025-04-22
DOI
https://doi.org/10.1109/tcbbio.2025.3562597
Citations
3
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
2.42

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article

Comparison of Deep-Learning Models for Classification of Cellular Phenotype From Flow Cytometry Data

Aaron Chuah, Thomas Hewitt, Benjamin S. Mashford, T. Daniel Andrews et al.
3 citations
IEEE Transactions on Computational Biology and Bioinformatics
Single-cell and spatial transcriptomics
2.42
article

Comparison of Deep-Learning Models for Classification of Cellular Phenotype From Flow Cytometry Data

Aaron Chuah, Thomas Hewitt, Benjamin S. Mashford, T. Daniel Andrews, Maryam May
article en
3 citations

Abstract

This study compares the relative utility of deep learning models as automated phenotypic classifiers, built with features of peripheral blood cell populations assayed with flow cytometry. We report surprisingly good sensitively for the task of distinguishing male from female mice solely from attributes of cells present in peripheral blood samples. This novel application of cytometry technology is easily validated and represents an example use that is not reliably possible with current visual analysis techniques. It serves as a useful test case with known ground truth labels of a subtle cellular phenotype and indicates the potential of this approach to more biologically meaningful phenotypes. We evaluate three different deep neural network architectures that vary in how the high-dimensional flow cytometry data is processed as input: 1) a convolutional neural network applied to the raw, per-cell marker intensity values, 2) a multi-layer perceptron taking per-channel histograms representing the range of intensities for a given marker, and 3) a multi-layer perceptron using a hypervoxel representation of the set of marker intensities for each cell in a given input sample. Our results show the histogram-based multi-layer perceptron achieves the highest classification accuracy of 91% on 2300 mouse blood samples for a mutant phenotype classification task. This indicates the value of deep learning models for detection of subtle signals that are not readily observed in high dimensions by visual analysis. These results demonstrate the effectiveness of deep learning for automated analysis of flow cytometry data on a challenging and biologically complex classification task.

IEEE Transactions on Computational Biology and BioinformaticsVol. 22(4)
Australian National University (AU), National Cancer Centre Singapore (SG)
National Institutes of Health
Openalex Percentile: Top 12%
Single-cell and spatial transcriptomics
2.42
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