TockyLocus: Quantitative Analysis Methods for Flow Cytometric Fluorescent Timer Data
Masahiro Ono

TL;DR
This paper introduces the TockyLocus R package with algorithms for quantitative analysis of Fluorescent Timer data, improving the interpretation of cellular dynamics captured by Tocky tools in flow cytometry.
Contribution
It presents a novel data categorization method and an R package for standardized, quantitative analysis of Fluorescent Timer flow cytometry data, enhancing biological insights.
Findings
The five-locus approach effectively captures Timer profile dynamics.
The TockyLocus package enables standardized data analysis and visualization.
Algorithms improve the interpretation of cellular temporal changes.
Abstract
Fluorescent Timer proteins, which spontaneously change their emission spectra over time, are valuable tools for analyzing temporal changes in cellular activities at the single-cell level. Traditional analysis of Fluorescent Timer data has mostly relied on conventional flow cytometric methods, which lacks the sophistication needed for detailed quantitative analysis. Recently, we developed the Timer-of-Cell-Kinetics-and-Activity (Tocky) tools, employing transgenic reporter systems using an mCherry mutant Timer protein, Fast-FT, to analyze these changes, implementing data preprocessing methods for Timer fluorescence. Despite this advancement, the computational implementation of effective quantitative analysis methods for Fluorescent Timer data has been lacking. In this study, we introduce rigorous algorithms for a data categorization method, designated as the Tocky locus approach, which…
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Taxonomy
TopicsSingle-cell and spatial transcriptomics
