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A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies
Author(s) -
Qihua Tan,
Mads Thomassen,
Jacob Hjelmborg,
Anders Clemmensen,
Klaus E. Andersen,
Thomas K. Petersen,
Matthew McGue,
Kaare Christensen,
Torben A. Kruse
Publication year - 2011
Publication title -
advances in bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.33
H-Index - 20
eISSN - 1687-8035
pISSN - 1687-8027
DOI - 10.1155/2011/261514
Subject(s) - computer science , expression (computer science) , microarray analysis techniques , gene expression , set (abstract data type) , gene chip analysis , curve fitting , parametric statistics , microarray , computational biology , gene , data mining , mathematics , statistics , biology , machine learning , genetics , programming language
Identifying the various gene expression response patterns is a challenging issue in expression microarray time-course experiments. Due to heterogeneity in the regulatory reaction among thousands of genes tested, it is impossible to manually characterize a parametric form for each of the time-course pattern in a gene by gene manner. We introduce a growth curve model with fractional polynomials to automatically capture the various time-dependent expression patterns and meanwhile efficiently handle missing values due to incomplete observations. For each gene, our procedure compares the performances among fractional polynomial models with power terms from a set of fixed values that offer a wide range of curve shapes and suggests a best fitting model. After a limited simulation study, the model has been applied to our human in vivo irritated epidermis data with missing observations to investigate time-dependent transcriptional responses to a chemical irritant. Our method was able to identify the various nonlinear time-course expression trajectories. The integration of growth curves with fractional polynomials provides a flexible way to model different time-course patterns together with model selection and significant gene identification strategies that can be applied in microarray-based time-course gene expression experiments with missing observations.

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