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Assessment of network module identification across complex diseases
Many bioinformatics methods have been proposed for reducing the complexity of large gene or protein networks into relevant subnetworks or modules. Yet, how such methods compare to each other in terms of their ability to identify disease-relevant modules in different types of network remains poorly u...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719725/ https://www.ncbi.nlm.nih.gov/pubmed/31471613 http://dx.doi.org/10.1038/s41592-019-0509-5 |
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author | Choobdar, Sarvenaz Ahsen, Mehmet E. Crawford, Jake Tomasoni, Mattia Fang, Tao Lamparter, David Lin, Junyuan Hescott, Benjamin Hu, Xiaozhe Mercer, Johnathan Natoli, Ted Narayan, Rajiv Subramanian, Aravind Zhang, Jitao D. Stolovitzky, Gustavo Kutalik, Zoltán Lage, Kasper Slonim, Donna K. Saez-Rodriguez, Julio Cowen, Lenore J. Bergmann, Sven Marbach, Daniel |
author_facet | Choobdar, Sarvenaz Ahsen, Mehmet E. Crawford, Jake Tomasoni, Mattia Fang, Tao Lamparter, David Lin, Junyuan Hescott, Benjamin Hu, Xiaozhe Mercer, Johnathan Natoli, Ted Narayan, Rajiv Subramanian, Aravind Zhang, Jitao D. Stolovitzky, Gustavo Kutalik, Zoltán Lage, Kasper Slonim, Donna K. Saez-Rodriguez, Julio Cowen, Lenore J. Bergmann, Sven Marbach, Daniel |
author_sort | Choobdar, Sarvenaz |
collection | PubMed |
description | Many bioinformatics methods have been proposed for reducing the complexity of large gene or protein networks into relevant subnetworks or modules. Yet, how such methods compare to each other in terms of their ability to identify disease-relevant modules in different types of network remains poorly understood. We launched the ‘Disease Module Identification DREAM Challenge’, an open competition to comprehensively assess module identification methods across diverse protein–protein interaction, signaling, gene co-expression, homology and cancer-gene networks. Predicted network modules were tested for association with complex traits and diseases using a unique collection of 180 genome-wide association studies. Our robust assessment of 75 module identification methods reveals top-performing algorithms, which recover complementary trait-associated modules. We find that most of these modules correspond to core disease-relevant pathways, which often comprise therapeutic targets. This community challenge establishes biologically interpretable benchmarks, tools and guidelines for molecular network analysis to study human disease biology. |
format | Online Article Text |
id | pubmed-6719725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-67197252019-10-11 Assessment of network module identification across complex diseases Choobdar, Sarvenaz Ahsen, Mehmet E. Crawford, Jake Tomasoni, Mattia Fang, Tao Lamparter, David Lin, Junyuan Hescott, Benjamin Hu, Xiaozhe Mercer, Johnathan Natoli, Ted Narayan, Rajiv Subramanian, Aravind Zhang, Jitao D. Stolovitzky, Gustavo Kutalik, Zoltán Lage, Kasper Slonim, Donna K. Saez-Rodriguez, Julio Cowen, Lenore J. Bergmann, Sven Marbach, Daniel Nat Methods Analysis Many bioinformatics methods have been proposed for reducing the complexity of large gene or protein networks into relevant subnetworks or modules. Yet, how such methods compare to each other in terms of their ability to identify disease-relevant modules in different types of network remains poorly understood. We launched the ‘Disease Module Identification DREAM Challenge’, an open competition to comprehensively assess module identification methods across diverse protein–protein interaction, signaling, gene co-expression, homology and cancer-gene networks. Predicted network modules were tested for association with complex traits and diseases using a unique collection of 180 genome-wide association studies. Our robust assessment of 75 module identification methods reveals top-performing algorithms, which recover complementary trait-associated modules. We find that most of these modules correspond to core disease-relevant pathways, which often comprise therapeutic targets. This community challenge establishes biologically interpretable benchmarks, tools and guidelines for molecular network analysis to study human disease biology. Nature Publishing Group US 2019-08-30 2019 /pmc/articles/PMC6719725/ /pubmed/31471613 http://dx.doi.org/10.1038/s41592-019-0509-5 Text en © The Author(s), under exclusive licence to Springer Nature America, Inc. 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Analysis Choobdar, Sarvenaz Ahsen, Mehmet E. Crawford, Jake Tomasoni, Mattia Fang, Tao Lamparter, David Lin, Junyuan Hescott, Benjamin Hu, Xiaozhe Mercer, Johnathan Natoli, Ted Narayan, Rajiv Subramanian, Aravind Zhang, Jitao D. Stolovitzky, Gustavo Kutalik, Zoltán Lage, Kasper Slonim, Donna K. Saez-Rodriguez, Julio Cowen, Lenore J. Bergmann, Sven Marbach, Daniel Assessment of network module identification across complex diseases |
title | Assessment of network module identification across complex diseases |
title_full | Assessment of network module identification across complex diseases |
title_fullStr | Assessment of network module identification across complex diseases |
title_full_unstemmed | Assessment of network module identification across complex diseases |
title_short | Assessment of network module identification across complex diseases |
title_sort | assessment of network module identification across complex diseases |
topic | Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719725/ https://www.ncbi.nlm.nih.gov/pubmed/31471613 http://dx.doi.org/10.1038/s41592-019-0509-5 |
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