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multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data
BACKGROUND: Gene co-expression networks represent modules of genes with shared biological function, and have been widely used to model biological pathways in gene expression data. Co-expression networks associated with a specific trait can be constructed and identified using weighted gene co-express...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039544/ https://www.ncbi.nlm.nih.gov/pubmed/36964502 http://dx.doi.org/10.1186/s12859-023-05233-z |
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author | Tommasini, Dario Fogel, Brent L. |
author_facet | Tommasini, Dario Fogel, Brent L. |
author_sort | Tommasini, Dario |
collection | PubMed |
description | BACKGROUND: Gene co-expression networks represent modules of genes with shared biological function, and have been widely used to model biological pathways in gene expression data. Co-expression networks associated with a specific trait can be constructed and identified using weighted gene co-expression network analysis (WGCNA), which is especially useful for the study of transcriptional signatures in disease. WGCNA networks are typically constructed using both disease and wildtype samples, so molecular pathways associated with disease are identified. However, it would be advantageous to study such co-expression networks in their disease context across spatiotemporal conditions, but currently there is no comprehensive software implementation for this type of analysis. RESULTS: Here, we introduce a WGCNA-based procedure, multiWGCNA, that is tailored to datasets with variable spatial or temporal traits. As well as constructing the combined network, multiWGCNA also generates a network for each condition separately, and subsequently maps these modules between and across designs, and performs relevant downstream analyses, including module-trait correlation and module preservation. When applied to astrocyte-specific RNA-sequencing (RNA-seq) data from various brain regions of mice with experimental autoimmune encephalitis, multiWGCNA resolved the de novo formation of the neurotoxic astrocyte transcriptional program exclusively in the disease setting. Using time-course RNA-seq from mice with tau pathology (rTg4510), we demonstrate how multiWGCNA can also be used to study the temporal evolution of pathological modules over the course of disease progression. CONCLUSION: The multiWGCNA R package can be applied to expression data with two dimensions, which is especially useful for the study of disease-associated modules across time or space. The source code and functions are freely available at: https://github.com/fogellab/multiWGCNA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05233-z. |
format | Online Article Text |
id | pubmed-10039544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100395442023-03-26 multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data Tommasini, Dario Fogel, Brent L. BMC Bioinformatics Software BACKGROUND: Gene co-expression networks represent modules of genes with shared biological function, and have been widely used to model biological pathways in gene expression data. Co-expression networks associated with a specific trait can be constructed and identified using weighted gene co-expression network analysis (WGCNA), which is especially useful for the study of transcriptional signatures in disease. WGCNA networks are typically constructed using both disease and wildtype samples, so molecular pathways associated with disease are identified. However, it would be advantageous to study such co-expression networks in their disease context across spatiotemporal conditions, but currently there is no comprehensive software implementation for this type of analysis. RESULTS: Here, we introduce a WGCNA-based procedure, multiWGCNA, that is tailored to datasets with variable spatial or temporal traits. As well as constructing the combined network, multiWGCNA also generates a network for each condition separately, and subsequently maps these modules between and across designs, and performs relevant downstream analyses, including module-trait correlation and module preservation. When applied to astrocyte-specific RNA-sequencing (RNA-seq) data from various brain regions of mice with experimental autoimmune encephalitis, multiWGCNA resolved the de novo formation of the neurotoxic astrocyte transcriptional program exclusively in the disease setting. Using time-course RNA-seq from mice with tau pathology (rTg4510), we demonstrate how multiWGCNA can also be used to study the temporal evolution of pathological modules over the course of disease progression. CONCLUSION: The multiWGCNA R package can be applied to expression data with two dimensions, which is especially useful for the study of disease-associated modules across time or space. The source code and functions are freely available at: https://github.com/fogellab/multiWGCNA. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05233-z. BioMed Central 2023-03-24 /pmc/articles/PMC10039544/ /pubmed/36964502 http://dx.doi.org/10.1186/s12859-023-05233-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Software Tommasini, Dario Fogel, Brent L. multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data |
title | multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data |
title_full | multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data |
title_fullStr | multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data |
title_full_unstemmed | multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data |
title_short | multiWGCNA: an R package for deep mining gene co-expression networks in multi-trait expression data |
title_sort | multiwgcna: an r package for deep mining gene co-expression networks in multi-trait expression data |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039544/ https://www.ncbi.nlm.nih.gov/pubmed/36964502 http://dx.doi.org/10.1186/s12859-023-05233-z |
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