Statistical classification of multivariate flow cytometry data analyzed by manual gating: Stem, progenitor, and epithelial marker expression in nonsmall cell lung cancer and normal lung. Issue 1 (13th December 2012)

• Record Type: Journal Article
• Authors: Normolle, Daniel P.; Donnenberg, Vera S.; Donnenberg, Albert D.
• Other Names: Donnenberg Vera S. sponsoringEditor.; Ulrich Henning sponsoringEditor.; Tárnok Attila sponsoringEditor.
• Is Part Of: Cytometry. Volume 83A:Issue 1(2013:Jan.)
• Page Start: 150
• Page End: 160
• Publication Date: 2012-12-13
• Subjects: multivariate analysis -- p > n problem -- elastic net -- lasso -- random forest -- diagonal linear discriminant analysis -- nonsmall cell lung cancer -- normal lung -- stem cells; Flow cytometry -- Periodicals; Imaging systems in biology -- Periodicals; Imaging systems in medicine -- Periodicals; Diagnostic imaging -- Periodicals; 571.605
• DOI: 10.1002/cyto.a.22240
• Languages: English
• ISSNs: 1552-4922

Abstract

Abstract: The use of supervised classification to extract markers from primary flow cytometry data is an emerging field that has made significant progress, spurred by the growing complexity of multidimensional flow cytometry. Whether the markers are extracted without supervision or by conventional gate and region methods, the number of candidate variables identified is typically larger than the number of specimens (p > n) and many variables are highly intercorrelated. Thus, comparison across groups or treatments to determine which markers are significant is challenging. Here, we utilized a data set in which 86 variables were created by conventional manual analysis of individual listmode data files, and compared the application of five multivariate classification methods to discern subtle differences between the stem/progenitor content of 35 nonsmall cell lung cancer and adjacent normal lung specimens. The methods compared include elastic‐net, lasso, random forest, diagonal linear discriminant analysis, and best single variable (best‐1). We described a broadly applicable methodology consisting of: 1) variable transformation and standardization; 2) visualization and assessment of correlation between variables; 3) selection of significant variables and modeling; and 4) characterization of the quality and stability of the model. The analysis yielded both validating results (tumors are aneuploid and have higher light scatter properties than normal lung), as well as leads that require followup: Cytokeratin+ CD133+ progenitors are present in normal lung but reduced in lung cancer; diploid (or pseudo‐diploid) CD117+CD44+ cells are more prevalent in tumor. We anticipate that the methods described here will be broadly applicable to a variety of multidimensional cytometry problems. © 2012 International Society for Advancement of Cytometry