CATALYST

CATALYST preprocesses and analyzes high-dimensional mass cytometry and flow cytometry (CyTOF/HDCyto) data by performing spillover compensation, normalization, clustering, and statistical modeling of cellular populations.


Key Features:

  • Spillover Compensation: Implements bead-based spillover compensation to model and correct signal interference between CyTOF channels.
  • Comprehensive Preprocessing Pipeline: Supports file concatenation, bead-based normalization, single-cell deconvolution, doublet and debris removal, live-cell gating, and batch correction.
  • SingleCellExperiment Integration: Organizes cytometry datasets within the SingleCellExperiment data structure for consistent downstream analysis.
  • Cell Population Identification: Applies FlowSOM clustering to identify cellular populations with optional manual merging of clusters.
  • Differential Cytometry Analysis: Performs statistical modeling using generalized linear mixed models (GLMMs) and linear mixed models (LMMs) to analyze cell population abundance and marker expression changes.
  • Quality Control Assessment: Provides modules to evaluate machine sensitivity, staining performance, and sample-level technical variation.

Scientific Applications:

  • Mass Cytometry Data Analysis: Processes and interprets CyTOF and high-dimensional cytometry datasets for single-cell studies.
  • Cell Population Profiling: Identifies and characterizes immune and cellular subpopulations in complex biological samples.
  • Differential Cytometry Studies: Detects changes in cellular abundance and signaling marker expression across experimental conditions.
  • Clinical and Systems Immunology Research: Supports large-scale cytometry analyses in heterogeneous tissues and clinical cohorts.

Methodology:

CATALYST performs bead-based spillover compensation, normalization, and quality control on cytometry data, organizes processed data within a SingleCellExperiment object, identifies cell populations using FlowSOM clustering, and applies generalized linear mixed models (GLMMs) or linear mixed models (LMMs) for differential analysis of population abundance and marker expression.

Topics

Collections

Details

License:
GPL-2.0
Tool Type:
library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
7/6/2018
Last Updated:
4/18/2021

Operations

Publications

Chevrier S, Crowell HL, Zanotelli VRT, Engler S, Robinson MD, Bodenmiller B. Compensation of Signal Spillover in Suspension and Imaging Mass Cytometry. Cell Syst. 2018 May 23;6(5):612-620.e5. doi:10.1016/j.cels.2018.02.010.

Nowicka M, Krieg C, Crowell HL, Weber LM, Hartmann FJ, Guglietta S, Becher B, Levesque MP, Robinson MD. CyTOF workflow: differential discovery in high-throughput high-dimensional cytometry datasets. F1000Res. 2017 May 26;6:748. doi:10.12688/f1000research.11622.3.

Crowell HL, Chevrier S, Jacobs A, Sivapatham S; Tumor Profiler Consortium; Bodenmiller B, Robinson MD. An R-based reproducible and user-friendly preprocessing pipeline for CyTOF data. F1000Res. 2020 Oct 22;9:1263. doi:10.12688/f1000research.26073.2.

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