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Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks
Self-expressiveness is a mathematical property that aims at characterizing the relationship between instances in a dataset. This property has been applied widely and successfully in computer-vision tasks, time-series analysis, and to infer underlying network structures in domains including protein s...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046116/ https://www.ncbi.nlm.nih.gov/pubmed/36979461 http://dx.doi.org/10.3390/biom13030526 |
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author | Peignier, Sergio Calevro, Federica |
author_facet | Peignier, Sergio Calevro, Federica |
author_sort | Peignier, Sergio |
collection | PubMed |
description | Self-expressiveness is a mathematical property that aims at characterizing the relationship between instances in a dataset. This property has been applied widely and successfully in computer-vision tasks, time-series analysis, and to infer underlying network structures in domains including protein signaling interactions and social-networks activity. Nevertheless, despite its potential, self-expressiveness has not been explicitly used to infer gene networks. In this article, we present Generalizable Gene Self-Expressive Networks, a new, interpretable, and generalization-aware formalism to model gene networks, and we propose two methods: GXN•EN and GXN•OMP, based respectively on [Formula: see text] and [Formula: see text] (Orthogonal Matching Pursuit), to infer and assess Generalizable Gene Self-Expressive Networks. We evaluate these methods on four Microarray datasets from the DREAM5 benchmark, using both internal and external metrics. The results obtained by both methods are comparable to those obtained by state-of-the-art tools, but are fast to train and exhibit high levels of sparsity, which make them easier to interpret. Moreover we applied these methods to three complex datasets containing RNA-seq informations from different mammalian tissues/cell-types. Lastly, we applied our methodology to compare a normal vs. a disease condition (Alzheimer), which allowed us to detect differential expression of genes’ sub-networks between these two biological conditions. Globally, the gene networks obtained exhibit a sparse and modular structure, with inner communities of genes presenting statistically significant over/under-expression on specific cell types, as well as significant enrichment for some anatomical GO terms, suggesting that such communities may also drive important functional roles. |
format | Online Article Text |
id | pubmed-10046116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100461162023-03-29 Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks Peignier, Sergio Calevro, Federica Biomolecules Article Self-expressiveness is a mathematical property that aims at characterizing the relationship between instances in a dataset. This property has been applied widely and successfully in computer-vision tasks, time-series analysis, and to infer underlying network structures in domains including protein signaling interactions and social-networks activity. Nevertheless, despite its potential, self-expressiveness has not been explicitly used to infer gene networks. In this article, we present Generalizable Gene Self-Expressive Networks, a new, interpretable, and generalization-aware formalism to model gene networks, and we propose two methods: GXN•EN and GXN•OMP, based respectively on [Formula: see text] and [Formula: see text] (Orthogonal Matching Pursuit), to infer and assess Generalizable Gene Self-Expressive Networks. We evaluate these methods on four Microarray datasets from the DREAM5 benchmark, using both internal and external metrics. The results obtained by both methods are comparable to those obtained by state-of-the-art tools, but are fast to train and exhibit high levels of sparsity, which make them easier to interpret. Moreover we applied these methods to three complex datasets containing RNA-seq informations from different mammalian tissues/cell-types. Lastly, we applied our methodology to compare a normal vs. a disease condition (Alzheimer), which allowed us to detect differential expression of genes’ sub-networks between these two biological conditions. Globally, the gene networks obtained exhibit a sparse and modular structure, with inner communities of genes presenting statistically significant over/under-expression on specific cell types, as well as significant enrichment for some anatomical GO terms, suggesting that such communities may also drive important functional roles. MDPI 2023-03-13 /pmc/articles/PMC10046116/ /pubmed/36979461 http://dx.doi.org/10.3390/biom13030526 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Peignier, Sergio Calevro, Federica Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks |
title | Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks |
title_full | Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks |
title_fullStr | Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks |
title_full_unstemmed | Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks |
title_short | Gene Self-Expressive Networks as a Generalization-Aware Tool to Model Gene Regulatory Networks |
title_sort | gene self-expressive networks as a generalization-aware tool to model gene regulatory networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10046116/ https://www.ncbi.nlm.nih.gov/pubmed/36979461 http://dx.doi.org/10.3390/biom13030526 |
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