Abstract

BackgroundModern flow cytometry technology has enabled the simultaneous analysis of multiple cell markers at the single-cell level, and it is widely used in a broad field of research. The detection of cell populations in flow cytometry data has long been dependent on “manual gating” by visual inspection. Recently, numerous software have been developed for automatic, computationally guided detection of cell populations; however, they are not designed for time-series flow cytometry data. Time-series flow cytometry data are indispensable for investigating the dynamics of cell populations that could not be elucidated by static time-point analysis. Therefore, there is a great need for tools to systematically analyze time-series flow cytometry data.ResultsWe propose a simple and efficient statistical framework, named CYBERTRACK (CYtometry-Based Estimation and Reasoning for TRACKing cell populations), to perform clustering and cell population tracking for time-series flow cytometry data. CYBERTRACK assumes that flow cytometry data are generated from a multivariate Gaussian mixture distribution with its mixture proportion at the current time dependent on that at a previous timepoint. Using simulation data, we evaluate the performance of CYBERTRACK when estimating parameters for a multivariate Gaussian mixture distribution, tracking time-dependent transitions of mixture proportions, and detecting change-points in the overall mixture proportion. The CYBERTRACK performance is validated using two real flow cytometry datasets, which demonstrate that the population dynamics detected by CYBERTRACK are consistent with our prior knowledge of lymphocyte behavior.ConclusionsOur results indicate that CYBERTRACK offers better understandings of time-dependent cell population dynamics to cytometry users by systematically analyzing time-series flow cytometry data.

Highlights

  • Modern flow cytometry technology has enabled the simultaneous analysis of multiple cell markers at the single-cell level, and it is widely used in a broad field of research

  • Time-series flow cytometry data offer information on longitudinal cell population dynamics that could not be elucidated by conventional static time-point data

  • We provide a simple and efficient learning procedure for the proposed model by using a stochastic EM algorithm, which is an alternate iteration of Gibbs sampling and maximum a posteriori (MAP) estimation of parameters

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Summary

Introduction

Modern flow cytometry technology has enabled the simultaneous analysis of multiple cell markers at the single-cell level, and it is widely used in a broad field of research. Minoura et al BMC Bioinformatics 2019, 20(Suppl 23):633 plot, but it suffers from several major limitations, including subjectivity, operator bias, difficulties in detecting unknown cell populations, and difficulties in reproducibility [4–6] To overcome these limitations, several methods have been proposed for the computationally guided or automated detection of unknown cell populations by unsupervised clustering, including FlowSOM, X-shift, PhenoGraph, Rclusterpp, and flowMeans [7]. Several methods have been proposed for the computationally guided or automated detection of unknown cell populations by unsupervised clustering, including FlowSOM, X-shift, PhenoGraph, Rclusterpp, and flowMeans [7] These methods have been successfully applied to identify both major and rare cell populations, they are not designed for modeling and analyzing time-series data and cannot capture the time-dependent properties and dynamics of cell populations. Such research is currently limited by a lack of a systematic mathematical framework to adequately model and analyze time-series flow cytometry data

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