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Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA)

Weighted gene co-expression network analysis (WGCNA) is used to detect clusters with highly correlated genes. Measurements of correlation most typically rely on linear relationships. However, a linear relationship does not always model pairwise functional-related dependence between genes. In this pa...

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Detalles Bibliográficos
Autores principales: Zhang, Tianjiao, Wong, Garry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307959/
https://www.ncbi.nlm.nih.gov/pubmed/35891798
http://dx.doi.org/10.1016/j.csbj.2022.07.018
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author Zhang, Tianjiao
Wong, Garry
author_facet Zhang, Tianjiao
Wong, Garry
author_sort Zhang, Tianjiao
collection PubMed
description Weighted gene co-expression network analysis (WGCNA) is used to detect clusters with highly correlated genes. Measurements of correlation most typically rely on linear relationships. However, a linear relationship does not always model pairwise functional-related dependence between genes. In this paper, we first compared 6 different correlation methods in their ability to capture complex dependence between genes in three different tissues. Next, we compared their gene-pairwise coefficient results and corresponding WGCNA results. Finally, we applied a recently proposed correlation method, Hellinger correlation, as a more sensitive correlation measurement in WGCNA. To test this method, we constructed gene networks containing co-expression gene modules from RNA-seq data of human frontal cortex from Alzheimer’s disease patients. To test the generality, we also used a microarray data set from human frontal cortex, single cell RNA-seq data from human prefrontal cortex, RNA-seq data from human temporal cortex, and GTEx data from heart. The Hellinger correlation method captures essentially similar results as other linear correlations in WGCNA, but provides additional new functional relationships as exemplified by uncovering a link between inflammation and mitochondria function. We validated the network constructed with the microarray and single cell sequencing data sets and a RNA-seq dataset of temporal cortex. We observed that this new correlation method enables the detection of non-linear biologically meaningful relationships among genes robustly and provides a complementary new approach to WGCNA. Thus, the application of Hellinger correlation to WGCNA provides a more flexible correlation approach to modelling networks in gene expression analysis that uncovers novel network relationships.
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spelling pubmed-93079592022-07-25 Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA) Zhang, Tianjiao Wong, Garry Comput Struct Biotechnol J Research Article Weighted gene co-expression network analysis (WGCNA) is used to detect clusters with highly correlated genes. Measurements of correlation most typically rely on linear relationships. However, a linear relationship does not always model pairwise functional-related dependence between genes. In this paper, we first compared 6 different correlation methods in their ability to capture complex dependence between genes in three different tissues. Next, we compared their gene-pairwise coefficient results and corresponding WGCNA results. Finally, we applied a recently proposed correlation method, Hellinger correlation, as a more sensitive correlation measurement in WGCNA. To test this method, we constructed gene networks containing co-expression gene modules from RNA-seq data of human frontal cortex from Alzheimer’s disease patients. To test the generality, we also used a microarray data set from human frontal cortex, single cell RNA-seq data from human prefrontal cortex, RNA-seq data from human temporal cortex, and GTEx data from heart. The Hellinger correlation method captures essentially similar results as other linear correlations in WGCNA, but provides additional new functional relationships as exemplified by uncovering a link between inflammation and mitochondria function. We validated the network constructed with the microarray and single cell sequencing data sets and a RNA-seq dataset of temporal cortex. We observed that this new correlation method enables the detection of non-linear biologically meaningful relationships among genes robustly and provides a complementary new approach to WGCNA. Thus, the application of Hellinger correlation to WGCNA provides a more flexible correlation approach to modelling networks in gene expression analysis that uncovers novel network relationships. Research Network of Computational and Structural Biotechnology 2022-07-13 /pmc/articles/PMC9307959/ /pubmed/35891798 http://dx.doi.org/10.1016/j.csbj.2022.07.018 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Zhang, Tianjiao
Wong, Garry
Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA)
title Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA)
title_full Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA)
title_fullStr Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA)
title_full_unstemmed Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA)
title_short Gene expression data analysis using Hellinger correlation in weighted gene co-expression networks (WGCNA)
title_sort gene expression data analysis using hellinger correlation in weighted gene co-expression networks (wgcna)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307959/
https://www.ncbi.nlm.nih.gov/pubmed/35891798
http://dx.doi.org/10.1016/j.csbj.2022.07.018
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