Supervised Machine Learning for Cell Classification in Microwave Flow Cytometers

Microwave sensing of biological cells is of great interest for its noncontact, noninvasive nature and high-sensitivity, high-resolution potential. Nevertheless, the lack of measurement specificity has been a critical problem. In this work, we show that highly reproducible, unbiased microwave data of single cells, analyzed by classical machine learning (ML) algorithms, enable effective cell classification. Yeast cells, including Saccharomyces cerevisiae, Saccharomyces pastorianus, Candida albicans, Candida tropicalis, Candida parapsilosis, and Candida krusei, were measured with microwave flow cytometers at frequencies between 0.265 and 7.65 GHz. Four sets of yeast cell data with 7941, 310, 130, and 200 cells were obtained. ML models, including random forest, XGBoost, K-neighbors, decision tree, and support vector machine (SVM), were trained to classify cell types and viability. Accuracies of up to 86.3% were obtained for cell type classification. The results show that the addition of computer vision features via cell imaging helps improve accuracy and that ML model performance depends on its targeted cell traits, the number of frequencies applied, and the values of chosen frequencies. Standardized data acquisition and significantly more cell data are needed for further ML classification investigation.

Authors

Institutions

Publication Details

Journal
IEEE Sensors Journal
Published
2025-03-24
DOI
https://doi.org/10.1109/jsen.2025.3551914
Primary Topic
Millimeter-Wave Propagation and Modeling
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Supervised Machine Learning for Cell Classification in Microwave Flow Cytometers

Jeffrey A. Osterberg, Carl Ehrett, Benjamin Braun, Neelima Dahal et al.
IEEE Sensors Journal
Millimeter-Wave Propagation and Modeling
article

Supervised Machine Learning for Cell Classification in Microwave Flow Cytometers

Jeffrey A. Osterberg, Carl Ehrett, Benjamin Braun, Neelima Dahal, Nitya Harikumar, Pingshan Wang, Matthew Keagle
article en

Abstract

Microwave sensing of biological cells is of great interest for its noncontact, noninvasive nature and high-sensitivity, high-resolution potential. Nevertheless, the lack of measurement specificity has been a critical problem. In this work, we show that highly reproducible, unbiased microwave data of single cells, analyzed by classical machine learning (ML) algorithms, enable effective cell classification. Yeast cells, including Saccharomyces cerevisiae, Saccharomyces pastorianus, Candida albicans, Candida tropicalis, Candida parapsilosis, and Candida krusei, were measured with microwave flow cytometers at frequencies between 0.265 and 7.65 GHz. Four sets of yeast cell data with 7941, 310, 130, and 200 cells were obtained. ML models, including random forest, XGBoost, K-neighbors, decision tree, and support vector machine (SVM), were trained to classify cell types and viability. Accuracies of up to 86.3% were obtained for cell type classification. The results show that the addition of computer vision features via cell imaging helps improve accuracy and that ML model performance depends on its targeted cell traits, the number of frequencies applied, and the values of chosen frequencies. Standardized data acquisition and significantly more cell data are needed for further ML classification investigation.

IEEE Sensors JournalVol. 25(10)
Clemson University (US)
Army Research Office
Openalex Percentile: Top 95%
Millimeter-Wave Propagation and Modeling
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.