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 in | Cytometry. Part A Vol. 89; no. 1; pp. 59 - 70 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 |
AuthorAffiliation_xml | – name: 6 Department of Electrical and Computer Engineering University of Rochester – name: 5 Department of Medicine Emory University School of Medicine Atlanta Georgia – name: 2 Department of Biostatistics and Computational Biology University of Rochester, Rochester, New York – name: 3 Department of Microbiology and Immunology University of Rochester – name: 1 David H. Smith Center for Vaccine Biology and Immunology University of Rochester Medical Center, Rochester, New York – name: 4 Department of Medicine University of Rochester |
Author_xml | – sequence: 1 givenname: Jonathan A. surname: Rebhahn fullname: Rebhahn, Jonathan A. organization: University of Rochester Medical Center, Rochester, New York – sequence: 2 givenname: David R. surname: Roumanes fullname: Roumanes, David R. organization: University of Rochester Medical Center, Rochester, New York – sequence: 3 givenname: Yilin surname: Qi fullname: Qi, Yilin organization: University of Rochester Medical Center, Rochester, New York – sequence: 4 givenname: Atif surname: Khan fullname: Khan, Atif organization: University of Rochester, Rochester, New York – sequence: 5 givenname: Juilee surname: Thakar fullname: Thakar, Juilee organization: University of Rochester – sequence: 6 givenname: Alex surname: Rosenberg fullname: Rosenberg, Alex organization: University of Rochester – sequence: 7 givenname: F. Eun‐Hyung surname: Lee fullname: Lee, F. Eun‐Hyung organization: Emory University School of Medicine – sequence: 8 givenname: Sally A. surname: Quataert fullname: Quataert, Sally A. organization: University of Rochester Medical Center, Rochester, New York – sequence: 9 givenname: Gaurav surname: Sharma fullname: Sharma, Gaurav organization: University of Rochester – sequence: 10 givenname: Tim R. surname: Mosmann fullname: Mosmann, Tim R. organization: University of Rochester |
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CitedBy_id | crossref_primary_10_1002_eji_201646632 crossref_primary_10_1038_s41598_020_58326_7 crossref_primary_10_3389_fimmu_2017_00858 crossref_primary_10_1002_eji_201970107 crossref_primary_10_1038_nri_2016_56 crossref_primary_10_1002_cyto_a_24307 crossref_primary_10_1371_journal_pone_0205291 crossref_primary_10_3389_fimmu_2024_1347926 crossref_primary_10_1002_cyto_a_24320 crossref_primary_10_1016_j_vaccine_2017_07_115 crossref_primary_10_1111_all_16489 |
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Keywords | template immunophenotyping competitive clustering SWIFT sample comparison flow cytometry automated analysis EM algorithm |
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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 |
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