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Identification of gene pairs through penalized regression subject to constraints
BACKGROUND: This article concerns the identification of gene pairs or combinations of gene pairs associated with biological phenotype or clinical outcome, allowing for building predictive models that are not only robust to normalization but also easily validated and measured by qPCR techniques. Howe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670721/ https://www.ncbi.nlm.nih.gov/pubmed/29100492 http://dx.doi.org/10.1186/s12859-017-1872-9 |
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author | Shen, Rex Luo, Lan Jiang, Hui |
author_facet | Shen, Rex Luo, Lan Jiang, Hui |
author_sort | Shen, Rex |
collection | PubMed |
description | BACKGROUND: This article concerns the identification of gene pairs or combinations of gene pairs associated with biological phenotype or clinical outcome, allowing for building predictive models that are not only robust to normalization but also easily validated and measured by qPCR techniques. However, given a small number of biological samples yet a large number of genes, this problem suffers from the difficulty of high computational complexity and imposes challenges to the accuracy of identification statistically. RESULTS: In this paper, we propose a parsimonious model representation and develop efficient algorithms for identification. Particularly, we derive an equivalent model subject to a sum-to-zero constraint in penalized linear regression, where the correspondence between nonzero coefficients in these models is established. Most importantly, it reduces the model complexity of the traditional approach from the quadratic order to the linear order in the number of candidate genes, while overcoming the difficulty of model nonidentifiablity. Computationally, we develop an algorithm using the alternating direction method of multipliers (ADMM) to deal with the constraint. Numerically, we demonstrate that the proposed method outperforms the traditional method in terms of the statistical accuracy. Moreover, we demonstrate that our ADMM algorithm is more computationally efficient than a coordinate descent algorithm with a local search. Finally, we illustrate the proposed method on a prostate cancer dataset to identify gene pairs that are associated with pre-operative prostate-specific antigen. CONCLUSION: Our findings demonstrate the feasibility and utility of using gene pairs as biomarkers. |
format | Online Article Text |
id | pubmed-5670721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56707212017-11-15 Identification of gene pairs through penalized regression subject to constraints Shen, Rex Luo, Lan Jiang, Hui BMC Bioinformatics Methodology Article BACKGROUND: This article concerns the identification of gene pairs or combinations of gene pairs associated with biological phenotype or clinical outcome, allowing for building predictive models that are not only robust to normalization but also easily validated and measured by qPCR techniques. However, given a small number of biological samples yet a large number of genes, this problem suffers from the difficulty of high computational complexity and imposes challenges to the accuracy of identification statistically. RESULTS: In this paper, we propose a parsimonious model representation and develop efficient algorithms for identification. Particularly, we derive an equivalent model subject to a sum-to-zero constraint in penalized linear regression, where the correspondence between nonzero coefficients in these models is established. Most importantly, it reduces the model complexity of the traditional approach from the quadratic order to the linear order in the number of candidate genes, while overcoming the difficulty of model nonidentifiablity. Computationally, we develop an algorithm using the alternating direction method of multipliers (ADMM) to deal with the constraint. Numerically, we demonstrate that the proposed method outperforms the traditional method in terms of the statistical accuracy. Moreover, we demonstrate that our ADMM algorithm is more computationally efficient than a coordinate descent algorithm with a local search. Finally, we illustrate the proposed method on a prostate cancer dataset to identify gene pairs that are associated with pre-operative prostate-specific antigen. CONCLUSION: Our findings demonstrate the feasibility and utility of using gene pairs as biomarkers. BioMed Central 2017-11-03 /pmc/articles/PMC5670721/ /pubmed/29100492 http://dx.doi.org/10.1186/s12859-017-1872-9 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Shen, Rex Luo, Lan Jiang, Hui Identification of gene pairs through penalized regression subject to constraints |
title | Identification of gene pairs through penalized regression subject to constraints |
title_full | Identification of gene pairs through penalized regression subject to constraints |
title_fullStr | Identification of gene pairs through penalized regression subject to constraints |
title_full_unstemmed | Identification of gene pairs through penalized regression subject to constraints |
title_short | Identification of gene pairs through penalized regression subject to constraints |
title_sort | identification of gene pairs through penalized regression subject to constraints |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670721/ https://www.ncbi.nlm.nih.gov/pubmed/29100492 http://dx.doi.org/10.1186/s12859-017-1872-9 |
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