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Gene relevance based on multiple evidences in complex networks

MOTIVATION: Multi-omics approaches offer the opportunity to reconstruct a more complete picture of the molecular events associated with human diseases, but pose challenges in data analysis. Network-based methods for the analysis of multi-omics leverage the complex web of macromolecular interactions...

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Autores principales: Di Nanni, Noemi, Gnocchi, Matteo, Moscatelli, Marco, Milanesi, Luciano, Mosca, Ettore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883679/
https://www.ncbi.nlm.nih.gov/pubmed/31504182
http://dx.doi.org/10.1093/bioinformatics/btz652
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author Di Nanni, Noemi
Gnocchi, Matteo
Moscatelli, Marco
Milanesi, Luciano
Mosca, Ettore
author_facet Di Nanni, Noemi
Gnocchi, Matteo
Moscatelli, Marco
Milanesi, Luciano
Mosca, Ettore
author_sort Di Nanni, Noemi
collection PubMed
description MOTIVATION: Multi-omics approaches offer the opportunity to reconstruct a more complete picture of the molecular events associated with human diseases, but pose challenges in data analysis. Network-based methods for the analysis of multi-omics leverage the complex web of macromolecular interactions occurring within cells to extract significant patterns of molecular alterations. Existing network-based approaches typically address specific combinations of omics and are limited in terms of the number of layers that can be jointly analysed. In this study, we investigate the application of network diffusion to quantify gene relevance on the basis of multiple evidences (layers). RESULTS: We introduce a gene score (mND) that quantifies the relevance of a gene in a biological process taking into account the network proximity of the gene and its first neighbours to other altered genes. We show that mND has a better performance over existing methods in finding altered genes in network proximity in one or more layers. We also report good performances in recovering known cancer genes. The pipeline described in this article is broadly applicable, because it can handle different types of inputs: in addition to multi-omics datasets, datasets that are stratified in many classes (e.g., cell clusters emerging from single cell analyses) or a combination of the two scenarios. AVAILABILITY AND IMPLEMENTATION: The R package ‘mND’ is available at URL: https://www.itb.cnr.it/mnd. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-98836792023-01-31 Gene relevance based on multiple evidences in complex networks Di Nanni, Noemi Gnocchi, Matteo Moscatelli, Marco Milanesi, Luciano Mosca, Ettore Bioinformatics Original Papers MOTIVATION: Multi-omics approaches offer the opportunity to reconstruct a more complete picture of the molecular events associated with human diseases, but pose challenges in data analysis. Network-based methods for the analysis of multi-omics leverage the complex web of macromolecular interactions occurring within cells to extract significant patterns of molecular alterations. Existing network-based approaches typically address specific combinations of omics and are limited in terms of the number of layers that can be jointly analysed. In this study, we investigate the application of network diffusion to quantify gene relevance on the basis of multiple evidences (layers). RESULTS: We introduce a gene score (mND) that quantifies the relevance of a gene in a biological process taking into account the network proximity of the gene and its first neighbours to other altered genes. We show that mND has a better performance over existing methods in finding altered genes in network proximity in one or more layers. We also report good performances in recovering known cancer genes. The pipeline described in this article is broadly applicable, because it can handle different types of inputs: in addition to multi-omics datasets, datasets that are stratified in many classes (e.g., cell clusters emerging from single cell analyses) or a combination of the two scenarios. AVAILABILITY AND IMPLEMENTATION: The R package ‘mND’ is available at URL: https://www.itb.cnr.it/mnd. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-08-22 /pmc/articles/PMC9883679/ /pubmed/31504182 http://dx.doi.org/10.1093/bioinformatics/btz652 Text en © The Author(s) 2019. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Di Nanni, Noemi
Gnocchi, Matteo
Moscatelli, Marco
Milanesi, Luciano
Mosca, Ettore
Gene relevance based on multiple evidences in complex networks
title Gene relevance based on multiple evidences in complex networks
title_full Gene relevance based on multiple evidences in complex networks
title_fullStr Gene relevance based on multiple evidences in complex networks
title_full_unstemmed Gene relevance based on multiple evidences in complex networks
title_short Gene relevance based on multiple evidences in complex networks
title_sort gene relevance based on multiple evidences in complex networks
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883679/
https://www.ncbi.nlm.nih.gov/pubmed/31504182
http://dx.doi.org/10.1093/bioinformatics/btz652
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