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Recursive regularization for inferring gene networks from time-course gene expression profiles
BACKGROUND: Inferring gene networks from time-course microarray experiments with vector autoregressive (VAR) model is the process of identifying functional associations between genes through multivariate time series. This problem can be cast as a variable selection problem in Statistics. One of the...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686685/ https://www.ncbi.nlm.nih.gov/pubmed/19386091 http://dx.doi.org/10.1186/1752-0509-3-41 |
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author | Shimamura, Teppei Imoto, Seiya Yamaguchi, Rui Fujita, André Nagasaki, Masao Miyano, Satoru |
author_facet | Shimamura, Teppei Imoto, Seiya Yamaguchi, Rui Fujita, André Nagasaki, Masao Miyano, Satoru |
author_sort | Shimamura, Teppei |
collection | PubMed |
description | BACKGROUND: Inferring gene networks from time-course microarray experiments with vector autoregressive (VAR) model is the process of identifying functional associations between genes through multivariate time series. This problem can be cast as a variable selection problem in Statistics. One of the promising methods for variable selection is the elastic net proposed by Zou and Hastie (2005). However, VAR modeling with the elastic net succeeds in increasing the number of true positives while it also results in increasing the number of false positives. RESULTS: By incorporating relative importance of the VAR coefficients into the elastic net, we propose a new class of regularization, called recursive elastic net, to increase the capability of the elastic net and estimate gene networks based on the VAR model. The recursive elastic net can reduce the number of false positives gradually by updating the importance. Numerical simulations and comparisons demonstrate that the proposed method succeeds in reducing the number of false positives drastically while keeping the high number of true positives in the network inference and achieves two or more times higher true discovery rate (the proportion of true positives among the selected edges) than the competing methods even when the number of time points is small. We also compared our method with various reverse-engineering algorithms on experimental data of MCF-7 breast cancer cells stimulated with two ErbB ligands, EGF and HRG. CONCLUSION: The recursive elastic net is a powerful tool for inferring gene networks from time-course gene expression profiles. |
format | Text |
id | pubmed-2686685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26866852009-05-27 Recursive regularization for inferring gene networks from time-course gene expression profiles Shimamura, Teppei Imoto, Seiya Yamaguchi, Rui Fujita, André Nagasaki, Masao Miyano, Satoru BMC Syst Biol Methodology Article BACKGROUND: Inferring gene networks from time-course microarray experiments with vector autoregressive (VAR) model is the process of identifying functional associations between genes through multivariate time series. This problem can be cast as a variable selection problem in Statistics. One of the promising methods for variable selection is the elastic net proposed by Zou and Hastie (2005). However, VAR modeling with the elastic net succeeds in increasing the number of true positives while it also results in increasing the number of false positives. RESULTS: By incorporating relative importance of the VAR coefficients into the elastic net, we propose a new class of regularization, called recursive elastic net, to increase the capability of the elastic net and estimate gene networks based on the VAR model. The recursive elastic net can reduce the number of false positives gradually by updating the importance. Numerical simulations and comparisons demonstrate that the proposed method succeeds in reducing the number of false positives drastically while keeping the high number of true positives in the network inference and achieves two or more times higher true discovery rate (the proportion of true positives among the selected edges) than the competing methods even when the number of time points is small. We also compared our method with various reverse-engineering algorithms on experimental data of MCF-7 breast cancer cells stimulated with two ErbB ligands, EGF and HRG. CONCLUSION: The recursive elastic net is a powerful tool for inferring gene networks from time-course gene expression profiles. BioMed Central 2009-04-22 /pmc/articles/PMC2686685/ /pubmed/19386091 http://dx.doi.org/10.1186/1752-0509-3-41 Text en Copyright © 2009 Shimamura et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Shimamura, Teppei Imoto, Seiya Yamaguchi, Rui Fujita, André Nagasaki, Masao Miyano, Satoru Recursive regularization for inferring gene networks from time-course gene expression profiles |
title | Recursive regularization for inferring gene networks from time-course gene expression profiles |
title_full | Recursive regularization for inferring gene networks from time-course gene expression profiles |
title_fullStr | Recursive regularization for inferring gene networks from time-course gene expression profiles |
title_full_unstemmed | Recursive regularization for inferring gene networks from time-course gene expression profiles |
title_short | Recursive regularization for inferring gene networks from time-course gene expression profiles |
title_sort | recursive regularization for inferring gene networks from time-course gene expression profiles |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686685/ https://www.ncbi.nlm.nih.gov/pubmed/19386091 http://dx.doi.org/10.1186/1752-0509-3-41 |
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