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Analysis of factorial time-course microarrays with application to a clinical study of burn injury

Authors :
Baiyu, Zhou
Weihong, Xu
David, Herndon
Ronald, Tompkins
Ronald, Davis
Wenzhong, Xiao
Wing Hung, Wong
Mehmet, Toner
H Shaw, Warren
David A, Schoenfeld
Laurence, Rahme
Grace P, McDonald-Smith
Douglas, Hayden
Philip, Mason
Shawn, Fagan
Yong-Ming, Yu
J Perren, Cobb
Daniel G, Remick
John A, Mannick
James A, Lederer
Richard L, Gamelli
Geoffrey M, Silver
Michael A, West
Michael B, Shapiro
Richard, Smith
David G, Camp
Weijun, Qian
John, Storey
Michael, Mindrinos
Rob, Tibshirani
Stephen, Lowry
Steven, Calvano
Irshad, Chaudry
Mitchell, Cohen
Ernest E, Moore
Jeffrey, Johnson
Lyle L, Moldawer
Henry V, Baker
Philip A, Efron
Ulysses G J, Balis
Timothy R, Billiar
Juan B, Ochoa
Jason L, Sperry
Carol L, Miller-Graziano
Asit K, De
Paul E, Bankey
Celeste C, Finnerty
Marc G, Jeschke
Joseph P, Minei
Brett D, Arnoldo
John L, Hunt
Jureta, Horton
Bernard, Brownstein
Bradley, Freeman
Ronald V, Maier
Avery B, Nathens
Joseph, Cuschieri
Nicole, Gibran
Matthew, Klein
Grant, O'Keefe
Source :
Proceedings of the National Academy of Sciences. 107:9923-9928
Publication Year :
2010
Publisher :
Proceedings of the National Academy of Sciences, 2010.

Abstract

Time-course microarray experiments are capable of capturing dynamic gene expression profiles. It is important to study how these dynamic profiles depend on the multiple factors that characterize the experimental condition under which the time course is observed. Analytic methods are needed to simultaneously handle the time course and factorial structure in the data. We developed a method to evaluate factor effects by pooling information across the time course while accounting for multiple testing and nonnormality of the microarray data. The method effectively extracts gene-specific response features and models their dependency on the experimental factors. Both longitudinal and cross-sectional time-course data can be handled by our approach. The method was used to analyze the impact of age on the temporal gene response to burn injury in a large-scale clinical study. Our analysis reveals that 21% of the genes responsive to burn are age-specific, among which expressions of mitochondria and immunoglobulin genes are differentially perturbed in pediatric and adult patients by burn injury. These new findings in the body’s response to burn injury between children and adults support further investigations of therapeutic options targeting specific age groups. The methodology proposed here has been implemented in R package “TANOVA” and submitted to the Comprehensive R Archive Network at http://www.r-project.org/ . It is also available for download at http://gluegrant1.stanford.edu/TANOVA/ .

Details

ISSN :
10916490 and 00278424
Volume :
107
Database :
OpenAIRE
Journal :
Proceedings of the National Academy of Sciences
Accession number :
edsair.doi.dedup.....3fd3e87f2480d0842fdd054860fd1e0c