Evidence map›Paper›PMID 25346887›Full record

ArticleTranslational cancer research2014

A recursively partitioned mixture model for clustering time-course gene expression data.

Devin C Koestler, Carmen J Marsit, Brock C Christensen, Karl T Kelsey, E Andres Houseman

Abstract read
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Article in Translational cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Devin C KoestlerDepartment of Biostatistics, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Carmen J MarsitDepartment of Community and Family Medicine, Section for Biostatistics and Epidemiology, Dartmouth Medical School, Hanover, New Hampshire 03756, USA ; Department of Pharmacology and Toxicology, Dartmouth College, Hanover, NH 03756, USA.
Brock C ChristensenDepartment of Community and Family Medicine, Section for Biostatistics and Epidemiology, Dartmouth Medical School, Hanover, New Hampshire 03756, USA ; Department of Pharmacology and Toxicology, Dartmouth College, Hanover, NH 03756, USA.
Karl T KelseyDepartment of Epidemiology, Brown University, Providence, RI 02192, USA.
E Andres HousemanDepartment of Public Health, Oregon State University, Corvallis, OR 97331, USA.

Funding

Heartland Institute for Clinical and Translational ResearchUL1TR000001 · NCATS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BAROHN, RICHARD J. · 2012 to 2015
$13.0M
The Boston Collaborative Oral Cancer StudyR01CA078609 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI KELSEY, KARL TIMOTHY · 1999 to 2010
$5.3M
Patterns of Somatic Gene Alterations in Oral CancerR01CA100679 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI KELSEY, KARL TIMOTHY · 2004 to 2012
$2.6M
Heartland Institute for Clinical and Translational ResearchKL2TR000119 · NCATS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BAROHN, RICHARD J. · 2012 to 2015
$2.5M
The Molecular Epidemiology of Bladder CancerR01CA121147 · NCI · BROWN UNIVERSITY · PI KELSEY, KARL TIMOTHY · 2007 to 2010
$2.0M
Model-Based Clustering of Genomic Data using Complex Covariance StructuresF31AG039190 · NIA · BROWN UNIVERSITY · PI KOESTLER, DEVIN CHARLES · 2010 to 2010
$22k
NCATS NIH HHS KL2 TR000119NCATS NIH HHS UL1 TR000001NCI NIH HHS R01 CA078609NCI NIH HHS R01 CA100679NCI NIH HHS R01 CA121147NIA NIH HHS F31 AG039190
6 · The paper itself

Abstract

backgroundLongitudinally collected gene expression data provides an opportunity to investigate the dynamic behavior of gene expression and is crucial for establishing causal links between changes on a molecular level and disease development and progression. In terms of the analysis of such data, clustering of subjects based on time-course expression data may improve our understanding of temporal expression patterns that result in disease phenotypes. Although there are numerous existing methods for clustering subjects using gene expression data, most are not suitable when expression measurements are repeatedly collected over a time-course.

methodsWe present a modified version of the recursively partitioned mixture model (RPMM) for clustering subjects based on longitudinally collected gene expression data. In the proposed time-course RPMM (TC-RPMM), subjects are clustered on the basis of their temporal profiles of gene expression using a mixture of mixed effects models framework. This framework captures changes in gene expression over time and models the autocorrelation between repeated gene expression measurements for the same subject. We assessed the performance of TC-RPMM using extensive simulation studies and a dataset from a multi-center research study of inflammation and response to injury (www.gluegrant.org), which consisted of time-course gene expression data for 140 subjects.

resultsOur simulation studies encompassed several different scenarios and were aimed at assessing the ability of TC-RPMM to correctly recover true class memberships when the expression trajectories that characterized those classes differed. Overall, our simulation studies revealed favorable performance of TC-RPMM compared to competing approaches, however clustering performance was observed to be highly dependent on the proportion of class discriminating genes used in clustering analysis. When applied to real epidemiologic data with repeated-measures, longitudinal gene expression measurements, TC-RPMM identified clusters that had strong biological and clinical significance.

conclusionsMethods for clustering subjects based on temporal gene expression profiles is a high priority for molecular biology and bioinformatics research. Along these lines, the proposed TC-RPMM represents a promising new approach for analyzing time-course gene expression data.

Indexed as

clusteringLongitudinal gene expression datamixture modelsrepeated-measures microarraystime-course microarrays

Identifiers

PMID25346887
PMCPMC4208690

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