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Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data

In biomedical applications, an experimenter encounters different potential sources of variation in data such as individual samples, multiple experimental conditions, and multivariate responses of a panel of markers such as from a signaling network. In multiparametric cytometry, which is often used f...

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Autores principales: Pyne, Saumyadipta, Lee, Sharon X., Wang, Kui, Irish, Jonathan, Tamayo, Pablo, Nazaire, Marc-Danie, Duong, Tarn, Ng, Shu-Kay, Hafler, David, Levy, Ronald, Nolan, Garry P., Mesirov, Jill, McLachlan, Geoffrey J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077578/
https://www.ncbi.nlm.nih.gov/pubmed/24983991
http://dx.doi.org/10.1371/journal.pone.0100334
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author Pyne, Saumyadipta
Lee, Sharon X.
Wang, Kui
Irish, Jonathan
Tamayo, Pablo
Nazaire, Marc-Danie
Duong, Tarn
Ng, Shu-Kay
Hafler, David
Levy, Ronald
Nolan, Garry P.
Mesirov, Jill
McLachlan, Geoffrey J.
author_facet Pyne, Saumyadipta
Lee, Sharon X.
Wang, Kui
Irish, Jonathan
Tamayo, Pablo
Nazaire, Marc-Danie
Duong, Tarn
Ng, Shu-Kay
Hafler, David
Levy, Ronald
Nolan, Garry P.
Mesirov, Jill
McLachlan, Geoffrey J.
author_sort Pyne, Saumyadipta
collection PubMed
description In biomedical applications, an experimenter encounters different potential sources of variation in data such as individual samples, multiple experimental conditions, and multivariate responses of a panel of markers such as from a signaling network. In multiparametric cytometry, which is often used for analyzing patient samples, such issues are critical. While computational methods can identify cell populations in individual samples, without the ability to automatically match them across samples, it is difficult to compare and characterize the populations in typical experiments, such as those responding to various stimulations or distinctive of particular patients or time-points, especially when there are many samples. Joint Clustering and Matching (JCM) is a multi-level framework for simultaneous modeling and registration of populations across a cohort. JCM models every population with a robust multivariate probability distribution. Simultaneously, JCM fits a random-effects model to construct an overall batch template – used for registering populations across samples, and classifying new samples. By tackling systems-level variation, JCM supports practical biomedical applications involving large cohorts. Software for fitting the JCM models have been implemented in an R package EMMIX-JCM, available from http://www.maths.uq.edu.au/~gjm/mix_soft/EMMIX-JCM/.
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spelling pubmed-40775782014-07-03 Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data Pyne, Saumyadipta Lee, Sharon X. Wang, Kui Irish, Jonathan Tamayo, Pablo Nazaire, Marc-Danie Duong, Tarn Ng, Shu-Kay Hafler, David Levy, Ronald Nolan, Garry P. Mesirov, Jill McLachlan, Geoffrey J. PLoS One Research Article In biomedical applications, an experimenter encounters different potential sources of variation in data such as individual samples, multiple experimental conditions, and multivariate responses of a panel of markers such as from a signaling network. In multiparametric cytometry, which is often used for analyzing patient samples, such issues are critical. While computational methods can identify cell populations in individual samples, without the ability to automatically match them across samples, it is difficult to compare and characterize the populations in typical experiments, such as those responding to various stimulations or distinctive of particular patients or time-points, especially when there are many samples. Joint Clustering and Matching (JCM) is a multi-level framework for simultaneous modeling and registration of populations across a cohort. JCM models every population with a robust multivariate probability distribution. Simultaneously, JCM fits a random-effects model to construct an overall batch template – used for registering populations across samples, and classifying new samples. By tackling systems-level variation, JCM supports practical biomedical applications involving large cohorts. Software for fitting the JCM models have been implemented in an R package EMMIX-JCM, available from http://www.maths.uq.edu.au/~gjm/mix_soft/EMMIX-JCM/. Public Library of Science 2014-07-01 /pmc/articles/PMC4077578/ /pubmed/24983991 http://dx.doi.org/10.1371/journal.pone.0100334 Text en © 2014 Pyne et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pyne, Saumyadipta
Lee, Sharon X.
Wang, Kui
Irish, Jonathan
Tamayo, Pablo
Nazaire, Marc-Danie
Duong, Tarn
Ng, Shu-Kay
Hafler, David
Levy, Ronald
Nolan, Garry P.
Mesirov, Jill
McLachlan, Geoffrey J.
Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data
title Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data
title_full Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data
title_fullStr Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data
title_full_unstemmed Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data
title_short Joint Modeling and Registration of Cell Populations in Cohorts of High-Dimensional Flow Cytometric Data
title_sort joint modeling and registration of cell populations in cohorts of high-dimensional flow cytometric data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077578/
https://www.ncbi.nlm.nih.gov/pubmed/24983991
http://dx.doi.org/10.1371/journal.pone.0100334
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