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Whole transcriptomic network analysis using Co-expression Differential Network Analysis (CoDiNA)

Whole transcriptomic network analysis using Co-expression Differential Network Analysis (CoDiNA)

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2451374869

Whole transcriptomic network analysis using Co-expression Differential Network Analysis (CoDiNA)

About this item

Full title

Whole transcriptomic network analysis using Co-expression Differential Network Analysis (CoDiNA)

Publisher

United States: Public Library of Science

Journal title

PloS one, 2020-10, Vol.15 (10), p.e0240523-e0240523

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Biological and medical sciences are increasingly acknowledging the significance of gene co-expression-networks for investigating complex-systems, phenotypes or diseases. Typically, complex phenotypes are investigated under varying conditions. While approaches for comparing nodes and links in two networks exist, almost no methods for the comparison of multiple networks are available and-to best of our knowledge-no comparative method allows for whole transcriptomic network analysis. However, it is the aim of many studies to compare networks of different conditions, for example, tissues, diseases, treatments, time points, or species. Here we present a method for the systematic comparison of an unlimited number of networks, with unlimited number of transcripts: Co-expression Differential Network Analysis (CoDiNA). In particular, CoDiNA detects links and nodes that are common, specific or different among the networks. We developed a statistical framework to normalize between these different categories of common or changed network links and nodes, resulting in a comprehensive network analysis method, more sophisticated than simply comparing the presence or absence of network nodes. Applying CoDiNA to a neurogenesis study we identified candidate genes involved in neuronal differentiation. We experimentally validated one candidate, demonstrating that its overexpression resulted in a significant disturbance in the underlying gene regulatory network of neurogenesis. Using clinical studies, we compared whole transcriptome co-expression networks from individuals with or without HIV and active tuberculosis (TB) and detected signature genes specific to HIV. Furthermore, analyzing multiple cancer transcription factor (TF) networks, we identified common and distinct features for particular cancer types. These CoDiNA applications demonstrate the successful detection of genes associated with specific phenotypes. Moreover, CoDiNA can also be used for comparing other types of undirected networks, for example, metabolic, protein-protein interaction, ecological and psychometric networks. CoDiNA is publicly available as an R package in CRAN (https://CRAN.R-project.org/package=CoDiNA)....

Alternative Titles

Full title

Whole transcriptomic network analysis using Co-expression Differential Network Analysis (CoDiNA)

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_2451374869

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2451374869

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0240523

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