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FERAL: network-based classifier with application to breast cancer outcome prediction

Motivation: Breast cancer outcome prediction based on gene expression profiles is an important strategy for personalize patient care. To improve performance and consistency of discovered markers of the initial molecular classifiers, network-based outcome prediction methods (NOPs) have been proposed....

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Detalles Bibliográficos
Autores principales: Allahyar, Amin, de Ridder, Jeroen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765883/
https://www.ncbi.nlm.nih.gov/pubmed/26072498
http://dx.doi.org/10.1093/bioinformatics/btv255
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author Allahyar, Amin
de Ridder, Jeroen
author_facet Allahyar, Amin
de Ridder, Jeroen
author_sort Allahyar, Amin
collection PubMed
description Motivation: Breast cancer outcome prediction based on gene expression profiles is an important strategy for personalize patient care. To improve performance and consistency of discovered markers of the initial molecular classifiers, network-based outcome prediction methods (NOPs) have been proposed. In spite of the initial claims, recent studies revealed that neither performance nor consistency can be improved using these methods. NOPs typically rely on the construction of meta-genes by averaging the expression of several genes connected in a network that encodes protein interactions or pathway information. In this article, we expose several fundamental issues in NOPs that impede on the prediction power, consistency of discovered markers and obscures biological interpretation. Results: To overcome these issues, we propose FERAL, a network-based classifier that hinges upon the Sparse Group Lasso which performs simultaneous selection of marker genes and training of the prediction model. An important feature of FERAL, and a significant departure from existing NOPs, is that it uses multiple operators to summarize genes into meta-genes. This gives the classifier the opportunity to select the most relevant meta-gene for each gene set. Extensive evaluation revealed that the discovered markers are markedly more stable across independent datasets. Moreover, interpretation of the marker genes detected by FERAL reveals valuable mechanistic insight into the etiology of breast cancer. Availability and implementation: All code is available for download at: http://homepage.tudelft.nl/53a60/resources/FERAL/FERAL.zip. Contact: j.deridder@tudelft.nl Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-47658832016-03-04 FERAL: network-based classifier with application to breast cancer outcome prediction Allahyar, Amin de Ridder, Jeroen Bioinformatics Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland Motivation: Breast cancer outcome prediction based on gene expression profiles is an important strategy for personalize patient care. To improve performance and consistency of discovered markers of the initial molecular classifiers, network-based outcome prediction methods (NOPs) have been proposed. In spite of the initial claims, recent studies revealed that neither performance nor consistency can be improved using these methods. NOPs typically rely on the construction of meta-genes by averaging the expression of several genes connected in a network that encodes protein interactions or pathway information. In this article, we expose several fundamental issues in NOPs that impede on the prediction power, consistency of discovered markers and obscures biological interpretation. Results: To overcome these issues, we propose FERAL, a network-based classifier that hinges upon the Sparse Group Lasso which performs simultaneous selection of marker genes and training of the prediction model. An important feature of FERAL, and a significant departure from existing NOPs, is that it uses multiple operators to summarize genes into meta-genes. This gives the classifier the opportunity to select the most relevant meta-gene for each gene set. Extensive evaluation revealed that the discovered markers are markedly more stable across independent datasets. Moreover, interpretation of the marker genes detected by FERAL reveals valuable mechanistic insight into the etiology of breast cancer. Availability and implementation: All code is available for download at: http://homepage.tudelft.nl/53a60/resources/FERAL/FERAL.zip. Contact: j.deridder@tudelft.nl Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2015-06-15 2015-06-10 /pmc/articles/PMC4765883/ /pubmed/26072498 http://dx.doi.org/10.1093/bioinformatics/btv255 Text en © The Author 2015. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland
Allahyar, Amin
de Ridder, Jeroen
FERAL: network-based classifier with application to breast cancer outcome prediction
title FERAL: network-based classifier with application to breast cancer outcome prediction
title_full FERAL: network-based classifier with application to breast cancer outcome prediction
title_fullStr FERAL: network-based classifier with application to breast cancer outcome prediction
title_full_unstemmed FERAL: network-based classifier with application to breast cancer outcome prediction
title_short FERAL: network-based classifier with application to breast cancer outcome prediction
title_sort feral: network-based classifier with application to breast cancer outcome prediction
topic Ismb/Eccb 2015 Proceedings Papers Committee July 10 to July 14, 2015, Dublin, Ireland
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4765883/
https://www.ncbi.nlm.nih.gov/pubmed/26072498
http://dx.doi.org/10.1093/bioinformatics/btv255
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