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Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs

MOTIVATION: The simultaneous availability of ATAC-seq and RNA-seq experiments allows to obtain a more in-depth knowledge on the regulatory mechanisms occurring in gene regulatory networks. In this article, we highlight and analyze two novel aspects that leverage on the possibility of pairing RNA-seq...

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Autores principales: Zenere, Alberto, Rundquist, Olof, Gustafsson, Mika, Altafini, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696094/
https://www.ncbi.nlm.nih.gov/pubmed/34383882
http://dx.doi.org/10.1093/bioinformatics/btab577
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author Zenere, Alberto
Rundquist, Olof
Gustafsson, Mika
Altafini, Claudio
author_facet Zenere, Alberto
Rundquist, Olof
Gustafsson, Mika
Altafini, Claudio
author_sort Zenere, Alberto
collection PubMed
description MOTIVATION: The simultaneous availability of ATAC-seq and RNA-seq experiments allows to obtain a more in-depth knowledge on the regulatory mechanisms occurring in gene regulatory networks. In this article, we highlight and analyze two novel aspects that leverage on the possibility of pairing RNA-seq and ATAC-seq data. Namely we investigate the causality of the relationships between transcription factors, chromatin and target genes and the internal consistency between the two omics, here measured in terms of structural balance in the sample correlations along elementary length-3 cycles. RESULTS: We propose a framework that uses the a priori knowledge on the data to infer elementary causal regulatory motifs (namely chains and forks) in the network. It is based on the notions of conditional independence and partial correlation, and can be applied to both longitudinal and non-longitudinal data. Our analysis highlights a strong connection between the causal regulatory motifs that are selected by the data and the structural balance of the underlying sample correlation graphs: strikingly, [Formula: see text] of the selected regulatory motifs belong to a balanced subgraph. This result shows that internal consistency, as measured by structural balance, is close to a necessary condition for 3-node regulatory motifs to satisfy causality rules. AVAILABILITY AND IMPLEMENTATION: The analysis was carried out in MATLAB and the code can be found at https://github.com/albertozenere/Multi-omics-elementary-regulatory-motifs. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-86960942022-01-04 Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs Zenere, Alberto Rundquist, Olof Gustafsson, Mika Altafini, Claudio Bioinformatics Original Papers MOTIVATION: The simultaneous availability of ATAC-seq and RNA-seq experiments allows to obtain a more in-depth knowledge on the regulatory mechanisms occurring in gene regulatory networks. In this article, we highlight and analyze two novel aspects that leverage on the possibility of pairing RNA-seq and ATAC-seq data. Namely we investigate the causality of the relationships between transcription factors, chromatin and target genes and the internal consistency between the two omics, here measured in terms of structural balance in the sample correlations along elementary length-3 cycles. RESULTS: We propose a framework that uses the a priori knowledge on the data to infer elementary causal regulatory motifs (namely chains and forks) in the network. It is based on the notions of conditional independence and partial correlation, and can be applied to both longitudinal and non-longitudinal data. Our analysis highlights a strong connection between the causal regulatory motifs that are selected by the data and the structural balance of the underlying sample correlation graphs: strikingly, [Formula: see text] of the selected regulatory motifs belong to a balanced subgraph. This result shows that internal consistency, as measured by structural balance, is close to a necessary condition for 3-node regulatory motifs to satisfy causality rules. AVAILABILITY AND IMPLEMENTATION: The analysis was carried out in MATLAB and the code can be found at https://github.com/albertozenere/Multi-omics-elementary-regulatory-motifs. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2021-08-12 /pmc/articles/PMC8696094/ /pubmed/34383882 http://dx.doi.org/10.1093/bioinformatics/btab577 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://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
Zenere, Alberto
Rundquist, Olof
Gustafsson, Mika
Altafini, Claudio
Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
title Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
title_full Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
title_fullStr Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
title_full_unstemmed Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
title_short Using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
title_sort using high-throughput multi-omics data to investigate structural balance in elementary gene regulatory network motifs
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8696094/
https://www.ncbi.nlm.nih.gov/pubmed/34383882
http://dx.doi.org/10.1093/bioinformatics/btab577
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