Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1784879556529750016 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9883679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT dinanninoemi generelevancebasedonmultipleevidencesincomplexnetworks AT gnocchimatteo generelevancebasedonmultipleevidencesincomplexnetworks AT moscatellimarco generelevancebasedonmultipleevidencesincomplexnetworks AT milanesiluciano generelevancebasedonmultipleevidencesincomplexnetworks AT moscaettore generelevancebasedonmultipleevidencesincomplexnetworks |