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Network-based integration of multi-omics data for prioritizing cancer genes

MOTIVATION: Several molecular events are known to be cancer-related, including genomic aberrations, hypermethylation of gene promoter regions and differential expression of microRNAs. These aberration events are very heterogeneous across tumors and it is poorly understood how they affect the molecul...

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Autores principales: Dimitrakopoulos, Christos, Hindupur, Sravanth Kumar, Häfliger, Luca, Behr, Jonas, Montazeri, Hesam, Hall, Michael N, Beerenwinkel, Niko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041755/
https://www.ncbi.nlm.nih.gov/pubmed/29547932
http://dx.doi.org/10.1093/bioinformatics/bty148
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author Dimitrakopoulos, Christos
Hindupur, Sravanth Kumar
Häfliger, Luca
Behr, Jonas
Montazeri, Hesam
Hall, Michael N
Beerenwinkel, Niko
author_facet Dimitrakopoulos, Christos
Hindupur, Sravanth Kumar
Häfliger, Luca
Behr, Jonas
Montazeri, Hesam
Hall, Michael N
Beerenwinkel, Niko
author_sort Dimitrakopoulos, Christos
collection PubMed
description MOTIVATION: Several molecular events are known to be cancer-related, including genomic aberrations, hypermethylation of gene promoter regions and differential expression of microRNAs. These aberration events are very heterogeneous across tumors and it is poorly understood how they affect the molecular makeup of the cell, including the transcriptome and proteome. Protein interaction networks can help decode the functional relationship between aberration events and changes in gene and protein expression. RESULTS: We developed NetICS (Network-based Integration of Multi-omics Data), a new graph diffusion-based method for prioritizing cancer genes by integrating diverse molecular data types on a directed functional interaction network. NetICS prioritizes genes by their mediator effect, defined as the proximity of the gene to upstream aberration events and to downstream differentially expressed genes and proteins in an interaction network. Genes are prioritized for individual samples separately and integrated using a robust rank aggregation technique. NetICS provides a comprehensive computational framework that can aid in explaining the heterogeneity of aberration events by their functional convergence to common differentially expressed genes and proteins. We demonstrate NetICS’ competitive performance in predicting known cancer genes and in generating robust gene lists using TCGA data from five cancer types. AVAILABILITY AND IMPLEMENTATION: NetICS is available at https://github.com/cbg-ethz/netics. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-60417552018-07-17 Network-based integration of multi-omics data for prioritizing cancer genes Dimitrakopoulos, Christos Hindupur, Sravanth Kumar Häfliger, Luca Behr, Jonas Montazeri, Hesam Hall, Michael N Beerenwinkel, Niko Bioinformatics Original Papers MOTIVATION: Several molecular events are known to be cancer-related, including genomic aberrations, hypermethylation of gene promoter regions and differential expression of microRNAs. These aberration events are very heterogeneous across tumors and it is poorly understood how they affect the molecular makeup of the cell, including the transcriptome and proteome. Protein interaction networks can help decode the functional relationship between aberration events and changes in gene and protein expression. RESULTS: We developed NetICS (Network-based Integration of Multi-omics Data), a new graph diffusion-based method for prioritizing cancer genes by integrating diverse molecular data types on a directed functional interaction network. NetICS prioritizes genes by their mediator effect, defined as the proximity of the gene to upstream aberration events and to downstream differentially expressed genes and proteins in an interaction network. Genes are prioritized for individual samples separately and integrated using a robust rank aggregation technique. NetICS provides a comprehensive computational framework that can aid in explaining the heterogeneity of aberration events by their functional convergence to common differentially expressed genes and proteins. We demonstrate NetICS’ competitive performance in predicting known cancer genes and in generating robust gene lists using TCGA data from five cancer types. AVAILABILITY AND IMPLEMENTATION: NetICS is available at https://github.com/cbg-ethz/netics. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2018-07-15 2018-03-14 /pmc/articles/PMC6041755/ /pubmed/29547932 http://dx.doi.org/10.1093/bioinformatics/bty148 Text en © The Author(s) 2018. 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 Original Papers
Dimitrakopoulos, Christos
Hindupur, Sravanth Kumar
Häfliger, Luca
Behr, Jonas
Montazeri, Hesam
Hall, Michael N
Beerenwinkel, Niko
Network-based integration of multi-omics data for prioritizing cancer genes
title Network-based integration of multi-omics data for prioritizing cancer genes
title_full Network-based integration of multi-omics data for prioritizing cancer genes
title_fullStr Network-based integration of multi-omics data for prioritizing cancer genes
title_full_unstemmed Network-based integration of multi-omics data for prioritizing cancer genes
title_short Network-based integration of multi-omics data for prioritizing cancer genes
title_sort network-based integration of multi-omics data for prioritizing cancer genes
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6041755/
https://www.ncbi.nlm.nih.gov/pubmed/29547932
http://dx.doi.org/10.1093/bioinformatics/bty148
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