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Optimized application of penalized regression methods to diverse genomic data
Motivation: Penalized regression methods have been adopted widely for high-dimensional feature selection and prediction in many bioinformatic and biostatistical contexts. While their theoretical properties are well-understood, specific methodology for their optimal application to genomic data has no...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232376/ https://www.ncbi.nlm.nih.gov/pubmed/22156367 http://dx.doi.org/10.1093/bioinformatics/btr591 |
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author | Waldron, Levi Pintilie, Melania Tsao, Ming-Sound Shepherd, Frances A. Huttenhower, Curtis Jurisica, Igor |
author_facet | Waldron, Levi Pintilie, Melania Tsao, Ming-Sound Shepherd, Frances A. Huttenhower, Curtis Jurisica, Igor |
author_sort | Waldron, Levi |
collection | PubMed |
description | Motivation: Penalized regression methods have been adopted widely for high-dimensional feature selection and prediction in many bioinformatic and biostatistical contexts. While their theoretical properties are well-understood, specific methodology for their optimal application to genomic data has not been determined. Results: Through simulation of contrasting scenarios of correlated high-dimensional survival data, we compared the LASSO, Ridge and Elastic Net penalties for prediction and variable selection. We found that a 2D tuning of the Elastic Net penalties was necessary to avoid mimicking the performance of LASSO or Ridge regression. Furthermore, we found that in a simulated scenario favoring the LASSO penalty, a univariate pre-filter made the Elastic Net behave more like Ridge regression, which was detrimental to prediction performance. We demonstrate the real-life application of these methods to predicting the survival of cancer patients from microarray data, and to classification of obese and lean individuals from metagenomic data. Based on these results, we provide an optimized set of guidelines for the application of penalized regression for reproducible class comparison and prediction with genomic data. Availability and Implementation: A parallelized implementation of the methods presented for regression and for simulation of synthetic data is provided as the pensim R package, available at http://cran.r-project.org/web/packages/pensim/index.html. Contact: chuttenh@hsph.harvard.edu; juris@ai.utoronto.ca Supplementary Information: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-3232376 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32323762011-12-07 Optimized application of penalized regression methods to diverse genomic data Waldron, Levi Pintilie, Melania Tsao, Ming-Sound Shepherd, Frances A. Huttenhower, Curtis Jurisica, Igor Bioinformatics Original Papers Motivation: Penalized regression methods have been adopted widely for high-dimensional feature selection and prediction in many bioinformatic and biostatistical contexts. While their theoretical properties are well-understood, specific methodology for their optimal application to genomic data has not been determined. Results: Through simulation of contrasting scenarios of correlated high-dimensional survival data, we compared the LASSO, Ridge and Elastic Net penalties for prediction and variable selection. We found that a 2D tuning of the Elastic Net penalties was necessary to avoid mimicking the performance of LASSO or Ridge regression. Furthermore, we found that in a simulated scenario favoring the LASSO penalty, a univariate pre-filter made the Elastic Net behave more like Ridge regression, which was detrimental to prediction performance. We demonstrate the real-life application of these methods to predicting the survival of cancer patients from microarray data, and to classification of obese and lean individuals from metagenomic data. Based on these results, we provide an optimized set of guidelines for the application of penalized regression for reproducible class comparison and prediction with genomic data. Availability and Implementation: A parallelized implementation of the methods presented for regression and for simulation of synthetic data is provided as the pensim R package, available at http://cran.r-project.org/web/packages/pensim/index.html. Contact: chuttenh@hsph.harvard.edu; juris@ai.utoronto.ca Supplementary Information: Supplementary data are available at Bioinformatics online. Oxford University Press 2011-12-15 2011-10-24 /pmc/articles/PMC3232376/ /pubmed/22156367 http://dx.doi.org/10.1093/bioinformatics/btr591 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Papers Waldron, Levi Pintilie, Melania Tsao, Ming-Sound Shepherd, Frances A. Huttenhower, Curtis Jurisica, Igor Optimized application of penalized regression methods to diverse genomic data |
title | Optimized application of penalized regression methods to diverse genomic data |
title_full | Optimized application of penalized regression methods to diverse genomic data |
title_fullStr | Optimized application of penalized regression methods to diverse genomic data |
title_full_unstemmed | Optimized application of penalized regression methods to diverse genomic data |
title_short | Optimized application of penalized regression methods to diverse genomic data |
title_sort | optimized application of penalized regression methods to diverse genomic data |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232376/ https://www.ncbi.nlm.nih.gov/pubmed/22156367 http://dx.doi.org/10.1093/bioinformatics/btr591 |
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