FlowSOM: Using self‐organizing maps for visualization and interpretation of cytometry data

The number of markers measured in both flow and mass cytometry keeps increasing steadily. Although this provides a wealth of information, it becomes infeasible to analyze these datasets manually. When using 2D scatter plots, the number of possible plots increases exponentially with the number of mar...

Full description

Saved in:
Bibliographic Details
Published inCytometry. Part A Vol. 87; no. 7; pp. 636 - 645
Main Authors Van Gassen, Sofie, Callebaut, Britt, Van Helden, Mary J., Lambrecht, Bart N., Demeester, Piet, Dhaene, Tom, Saeys, Yvan
Format Journal Article
LanguageEnglish
Published United States 01.07.2015
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The number of markers measured in both flow and mass cytometry keeps increasing steadily. Although this provides a wealth of information, it becomes infeasible to analyze these datasets manually. When using 2D scatter plots, the number of possible plots increases exponentially with the number of markers and therefore, relevant information that is present in the data might be missed. In this article, we introduce a new visualization technique, called FlowSOM, which analyzes Flow or mass cytometry data using a Self‐Organizing Map. Using a two‐level clustering and star charts, our algorithm helps to obtain a clear overview of how all markers are behaving on all cells, and to detect subsets that might be missed otherwise. R code is available at https://github.com/SofieVG/FlowSOM and will be made available at Bioconductor. © 2015 International Society for Advancement of Cytometry
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1552-4922
1552-4930
1552-4930
DOI:10.1002/cyto.a.22625