CytoBinning: Immunological insights from multi-dimensional data

PLoS One. 2018 Oct 31;13(10):e0205291. doi: 10.1371/journal.pone.0205291. eCollection 2018.

Abstract

New cytometric techniques continue to push the boundaries of multi-parameter quantitative data acquisition at the single-cell level particularly in immunology and medicine. Sophisticated analysis methods for such ever higher dimensional datasets are rapidly emerging, with advanced data representations and dimensional reduction approaches. However, these are not yet standardized and clinical scientists and cell biologists are not yet experienced in their interpretation. More fundamentally their range of statistical validity is not yet fully established. We therefore propose a new method for the automated and unbiased analysis of high-dimensional single cell datasets that is simple and robust, with the goal of reducing this complex information into a familiar 2D scatter plot representation that is of immediate utility to a range of biomedical and clinical settings. Using publicly available flow cytometry and mass cytometry datasets we demonstrate that this method (termed CytoBinning), recapitulates the results of traditional manual cytometric analyses and leads to new and testable hypotheses.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / immunology*
  • Biomarkers / analysis
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / immunology
  • CD8 Antigens / genetics
  • CD8 Antigens / immunology
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • Datasets as Topic
  • Female
  • Flow Cytometry / statistics & numerical data*
  • Gene Expression
  • Humans
  • Image Cytometry / statistics & numerical data*
  • Immunity, Innate
  • Male
  • Pattern Recognition, Automated / statistics & numerical data*
  • Receptors, CCR7 / genetics
  • Receptors, CCR7 / immunology
  • Single-Cell Analysis / methods
  • Single-Cell Analysis / statistics & numerical data*

Substances

  • Biomarkers
  • CCR7 protein, human
  • CD8 Antigens
  • Receptors, CCR7

Grants and funding

R.W.J.L. was supported by the National Institute for Health Research (NIHR) Biomedical Research Centre based at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, UK. The views expressed are those of the authors and not necessarily those of the National Health Service, the NIHR or the Department of Health. W.L. was partially supported by AFOSR grant FA9550-16-1-0052. Y.S. and B.C.D. were supported by the National Institutes of Health, National Eye Institute intramural research program. The content of this publication does not necessarily reflect the views or policies of the U.S. Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.