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A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies
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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182337/ https://www.ncbi.nlm.nih.gov/pubmed/21966290 http://dx.doi.org/10.1155/2011/261514 |
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author | Tan, Qihua Thomassen, Mads Hjelmborg, Jacob v. B. Clemmensen, Anders Andersen, Klaus Ejner Petersen, Thomas K. McGue, Matthew Christensen, Kaare Kruse, Torben A. |
author_facet | Tan, Qihua Thomassen, Mads Hjelmborg, Jacob v. B. Clemmensen, Anders Andersen, Klaus Ejner Petersen, Thomas K. McGue, Matthew Christensen, Kaare Kruse, Torben A. |
author_sort | Tan, Qihua |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3182337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31823372011-09-30 A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies Tan, Qihua Thomassen, Mads Hjelmborg, Jacob v. B. Clemmensen, Anders Andersen, Klaus Ejner Petersen, Thomas K. McGue, Matthew Christensen, Kaare Kruse, Torben A. Adv Bioinformatics Research Article 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. Hindawi Publishing Corporation 2011 2011-09-27 /pmc/articles/PMC3182337/ /pubmed/21966290 http://dx.doi.org/10.1155/2011/261514 Text en Copyright © 2011 Qihua Tan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tan, Qihua Thomassen, Mads Hjelmborg, Jacob v. B. Clemmensen, Anders Andersen, Klaus Ejner Petersen, Thomas K. McGue, Matthew Christensen, Kaare Kruse, Torben A. A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies |
title | A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies |
title_full | A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies |
title_fullStr | A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies |
title_full_unstemmed | A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies |
title_short | A Growth Curve Model with Fractional Polynomials for Analysing Incomplete Time-Course Data in Microarray Gene Expression Studies |
title_sort | growth curve model with fractional polynomials for analysing incomplete time-course data in microarray gene expression studies |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182337/ https://www.ncbi.nlm.nih.gov/pubmed/21966290 http://dx.doi.org/10.1155/2011/261514 |
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