FlowAnd: Comprehensive Computational Framework for Flow Cytometry Data Analysis

  • Lahesmaa Korpinen A
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Abstract

Flow cytometry is a widely used high-throughput measurement technology in basic research and diagnostics. Recently the amount of data generated from flow cytometry experiments has been increasing, both in sample numbers and the number of parameters measured per cell. These highly multivariate datasets have become too large for use with tools depending mainly on manual analysis. We have implemented a computational framework (FlowAnd) that is designed to analyze and integrate largescale, multi-color flow cytometry data. The tool implements methods for data importing, various transformations, several clustering algorithms for automatic clustering, visualization tools as well as straightforward statistical testing. We applied FlowAnd to a phosphoproteomics data set from 37 chronic myeloid leukemia patients treated with two kinase inhibitors. Our results indicate high concordance between automated gating using three clustering algorithms and manual gating. Analysis of more than 70 flow cytometry experiments demonstrate the utility of features in FlowAnd, such as a graphical tool for rapid validation of clustering results, in large-scale flow cytometry data analysis. The FlowAnd framework allows accurate, fast and well documented analysis of multidimensional flow cytometry experiments. It provides several clustering algorithms for automatic gating, the possibility to add novel tools in various programming languages, such as Java, R, Python or MATLAB in an environment amenable to high-performance computing. FlowAnd can also be easily modified to comply with various marker panels and parameter settings. FlowAnd, all data and user guide are freely available under GNU General Public License at http://csbi.ltdk.helsinki.fi/flowand.

Figures

  • Figure 1: FlowAnd overview: An overview figure of the steps in a full analysis of flow cytometry data. First data are preprocessed by applying compensation and a transformation to the data. Next the cells are filtered by clustering and selecting debris clusters out from the data. The third step is to identify cell populations from the data and this is done by first clustering the data and then applying a rule based method to label the clusters into populations. Finally once the correct populations have been identified, the data can be summarized in a report.
  • Table 1: Panels of fluorescence antibodies used for specific stimulation conditions. This table is adapted from [9].
  • Figure 2: Comparison of gating algorithms: Comparison of a) manual gating to automatic gating with b) flowMeans, c) SamSPECTRAL and d) FLAME clustering. FlowMeans and SamSPECTRAL identify the three populations relatively well, while the FLAME mixture modeling with t skew distribution identifies too many clusters.
  • Figure 3: Visualization of results of statistical testing: A. The results of manual gating for STAT3 in the lymphocyte populations of 37 individuals from four patient groups, healthy controls, patients at diagnosis, patients after imatinib treatment and patients after dasatinib treatment. B. The replicated experiment using FlowAnd and the semi-automated analysis pipeline.

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APA

Lahesmaa Korpinen, A. M. (2011). FlowAnd: Comprehensive Computational Framework for Flow Cytometry Data Analysis. Journal of Proteomics & Bioinformatics, 4(11). https://doi.org/10.4172/jpb.1000197

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