Competitive SWIFT cluster templates enhance detection of aging changes

Clustering‐based algorithms for automated analysis of flow cytometry datasets have achieved more efficient and objective analysis than manual processing. Clustering organizes flow cytometry data into subpopulations with substantially homogenous characteristics but does not directly address the impor...

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Published inCytometry. Part A Vol. 89; no. 1; pp. 59 - 70
Main Authors Rebhahn, Jonathan A., Roumanes, David R., Qi, Yilin, Khan, Atif, Thakar, Juilee, Rosenberg, Alex, Lee, F. Eun‐Hyung, Quataert, Sally A., Sharma, Gaurav, Mosmann, Tim R.
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.01.2016
John Wiley and Sons Inc
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Abstract Clustering‐based algorithms for automated analysis of flow cytometry datasets have achieved more efficient and objective analysis than manual processing. Clustering organizes flow cytometry data into subpopulations with substantially homogenous characteristics but does not directly address the important problem of identifying the salient differences in subpopulations between subjects and groups. Here, we address this problem by augmenting SWIFT—a mixture model based clustering algorithm reported previously. First, we show that SWIFT clustering using a “template” mixture model, in which all subpopulations are represented, identifies small differences in cell numbers per subpopulation between samples. Second, we demonstrate that resolution of inter‐sample differences is increased by “competition” wherein a joint model is formed by combining the mixture model templates obtained from different groups. In the joint model, clusters from individual groups compete for the assignment of cells, sharpening differences between samples, particularly differences representing subpopulation shifts that are masked under clustering with a single template model. The benefit of competition was demonstrated first with a semisynthetic dataset obtained by deliberately shifting a known subpopulation within an actual flow cytometry sample. Single templates correctly identified changes in the number of cells in the subpopulation, but only the competition method detected small changes in median fluorescence. In further validation studies, competition identified a larger number of significantly altered subpopulations between young and elderly subjects. This enrichment was specific, because competition between templates from consensus male and female samples did not improve the detection of age‐related differences. Several changes between the young and elderly identified by SWIFT template competition were consistent with known alterations in the elderly, and additional altered subpopulations were also identified. Alternative algorithms detected far fewer significantly altered clusters. Thus SWIFT template competition is a powerful approach to sharpen comparisons between selected groups in flow cytometry datasets. © 2015 The Authors. Published Wiley Periodicals Inc.
AbstractList Clustering-based algorithms for automated analysis of flow cytometry datasets have achieved more efficient and objective analysis than manual processing. Clustering organizes flow cytometry data into subpopulations with substantially homogenous characteristics but does not directly address the important problem of identifying the salient differences in subpopulations between subjects and groups. Here, we address this problem by augmenting SWIFT-a mixture model based clustering algorithm reported previously. First, we show that SWIFT clustering using a "template" mixture model, in which all subpopulations are represented, identifies small differences in cell numbers per subpopulation between samples. Second, we demonstrate that resolution of inter-sample differences is increased by "competition" wherein a joint model is formed by combining the mixture model templates obtained from different groups. In the joint model, clusters from individual groups compete for the assignment of cells, sharpening differences between samples, particularly differences representing subpopulation shifts that are masked under clustering with a single template model. The benefit of competition was demonstrated first with a semisynthetic dataset obtained by deliberately shifting a known subpopulation within an actual flow cytometry sample. Single templates correctly identified changes in the number of cells in the subpopulation, but only the competition method detected small changes in median fluorescence. In further validation studies, competition identified a larger number of significantly altered subpopulations between young and elderly subjects. This enrichment was specific, because competition between templates from consensus male and female samples did not improve the detection of age-related differences. Several changes between the young and elderly identified by SWIFT template competition were consistent with known alterations in the elderly, and additional altered subpopulations were also identified. Alternative algorithms detected far fewer significantly altered clusters. Thus SWIFT template competition is a powerful approach to sharpen comparisons between selected groups in flow cytometry datasets. copyright 2015 The Authors. Published Wiley Periodicals Inc.
Clustering-based algorithms for automated analysis of flow cytometry datasets have achieved more efficient and objective analysis than manual processing. Clustering organizes flow cytometry data into subpopulations with substantially homogenous characteristics but does not directly address the important problem of identifying the salient differences in subpopulations between subjects and groups. Here, we address this problem by augmenting SWIFT--a mixture model based clustering algorithm reported previously. First, we show that SWIFT clustering using a "template" mixture model, in which all subpopulations are represented, identifies small differences in cell numbers per subpopulation between samples. Second, we demonstrate that resolution of inter-sample differences is increased by "competition" wherein a joint model is formed by combining the mixture model templates obtained from different groups. In the joint model, clusters from individual groups compete for the assignment of cells, sharpening differences between samples, particularly differences representing subpopulation shifts that are masked under clustering with a single template model. The benefit of competition was demonstrated first with a semisynthetic dataset obtained by deliberately shifting a known subpopulation within an actual flow cytometry sample. Single templates correctly identified changes in the number of cells in the subpopulation, but only the competition method detected small changes in median fluorescence. In further validation studies, competition identified a larger number of significantly altered subpopulations between young and elderly subjects. This enrichment was specific, because competition between templates from consensus male and female samples did not improve the detection of age-related differences. Several changes between the young and elderly identified by SWIFT template competition were consistent with known alterations in the elderly, and additional altered subpopulations were also identified. Alternative algorithms detected far fewer significantly altered clusters. Thus SWIFT template competition is a powerful approach to sharpen comparisons between selected groups in flow cytometry datasets.
Clustering‐based algorithms for automated analysis of flow cytometry datasets have achieved more efficient and objective analysis than manual processing. Clustering organizes flow cytometry data into subpopulations with substantially homogenous characteristics but does not directly address the important problem of identifying the salient differences in subpopulations between subjects and groups. Here, we address this problem by augmenting SWIFT—a mixture model based clustering algorithm reported previously. First, we show that SWIFT clustering using a “template” mixture model, in which all subpopulations are represented, identifies small differences in cell numbers per subpopulation between samples. Second, we demonstrate that resolution of inter‐sample differences is increased by “competition” wherein a joint model is formed by combining the mixture model templates obtained from different groups. In the joint model, clusters from individual groups compete for the assignment of cells, sharpening differences between samples, particularly differences representing subpopulation shifts that are masked under clustering with a single template model. The benefit of competition was demonstrated first with a semisynthetic dataset obtained by deliberately shifting a known subpopulation within an actual flow cytometry sample. Single templates correctly identified changes in the number of cells in the subpopulation, but only the competition method detected small changes in median fluorescence. In further validation studies, competition identified a larger number of significantly altered subpopulations between young and elderly subjects. This enrichment was specific, because competition between templates from consensus male and female samples did not improve the detection of age‐related differences. Several changes between the young and elderly identified by SWIFT template competition were consistent with known alterations in the elderly, and additional altered subpopulations were also identified. Alternative algorithms detected far fewer significantly altered clusters. Thus SWIFT template competition is a powerful approach to sharpen comparisons between selected groups in flow cytometry datasets. © 2015 The Authors. Published Wiley Periodicals Inc.
Author Roumanes, David R.
Quataert, Sally A.
Qi, Yilin
Sharma, Gaurav
Khan, Atif
Rebhahn, Jonathan A.
Thakar, Juilee
Rosenberg, Alex
Lee, F. Eun‐Hyung
Mosmann, Tim R.
AuthorAffiliation 2 Department of Biostatistics and Computational Biology University of Rochester, Rochester, New York
6 Department of Electrical and Computer Engineering University of Rochester
4 Department of Medicine University of Rochester
5 Department of Medicine Emory University School of Medicine Atlanta Georgia
1 David H. Smith Center for Vaccine Biology and Immunology University of Rochester Medical Center, Rochester, New York
3 Department of Microbiology and Immunology University of Rochester
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Copyright 2015 The Authors. Cytometry Part A Published by Wiley Periodicals, Inc. on behalf of ISAC
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2016 International Society for Advancement of Cytometry
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Issue 1
Keywords template
immunophenotyping
competitive clustering
SWIFT
sample comparison
flow cytometry
automated analysis
EM algorithm
Language English
License Attribution-NonCommercial
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2015 The Authors. Cytometry Part A Published by Wiley Periodicals, Inc. on behalf of ISAC.
This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
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Snippet Clustering‐based algorithms for automated analysis of flow cytometry datasets have achieved more efficient and objective analysis than manual processing....
Clustering-based algorithms for automated analysis of flow cytometry datasets have achieved more efficient and objective analysis than manual processing....
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StartPage 59
SubjectTerms Adult
Aged
Aged, 80 and over
Aging
Algorithms
automated analysis
Biomarkers - analysis
Change detection
Cluster Analysis
Clustering
Clusters
Competition
competitive clustering
Computational Analysis of Flow Cytometry Data (PART II)
Computational Biology - methods
Cytometry
Data Interpretation, Statistical
Datasets
EM algorithm
Female
Flow cytometry
Flow Cytometry - methods
Fluorescence
Geriatrics
Humans
immunophenotyping
Immunophenotyping - methods
Leukocytes, Mononuclear - cytology
Leukocytes, Mononuclear - immunology
Male
Middle Aged
Older people
sample comparison
Sex Factors
Sharpening
Subpopulations
SWIFT
template
Young Adult
Title Competitive SWIFT cluster templates enhance detection of aging changes
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcyto.a.22740
https://www.ncbi.nlm.nih.gov/pubmed/26441030
https://www.proquest.com/docview/1958768831
https://www.proquest.com/docview/1761081257
https://www.proquest.com/docview/1776651718
https://pubmed.ncbi.nlm.nih.gov/PMC4737406
Volume 89
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