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Journal ArticleDOI

A General Framework for Weighted Gene Co-Expression Network Analysis

TLDR
A general framework for `soft' thresholding that assigns a connection weight to each gene pair is described and several node connectivity measures are introduced and provided empirical evidence that they can be important for predicting the biological significance of a gene.
Abstract
Gene co-expression networks are increasingly used to explore the system-level functionality of genes. The network construction is conceptually straightforward: nodes represent genes and nodes are connected if the corresponding genes are significantly co-expressed across appropriately chosen tissue samples. In reality, it is tricky to define the connections between the nodes in such networks. An important question is whether it is biologically meaningful to encode gene co-expression using binary information (connected=1, unconnected=0). We describe a general framework for ;soft' thresholding that assigns a connection weight to each gene pair. This leads us to define the notion of a weighted gene co-expression network. For soft thresholding we propose several adjacency functions that convert the co-expression measure to a connection weight. For determining the parameters of the adjacency function, we propose a biologically motivated criterion (referred to as the scale-free topology criterion). We generalize the following important network concepts to the case of weighted networks. First, we introduce several node connectivity measures and provide empirical evidence that they can be important for predicting the biological significance of a gene. Second, we provide theoretical and empirical evidence that the ;weighted' topological overlap measure (used to define gene modules) leads to more cohesive modules than its ;unweighted' counterpart. Third, we generalize the clustering coefficient to weighted networks. Unlike the unweighted clustering coefficient, the weighted clustering coefficient is not inversely related to the connectivity. We provide a model that shows how an inverse relationship between clustering coefficient and connectivity arises from hard thresholding. We apply our methods to simulated data, a cancer microarray data set, and a yeast microarray data set.

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Citations
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Journal ArticleDOI

Modeling the functional genomics of autism using human neurons

TL;DR: Primary normal human neuronal progenitors were differentiated into a post-mitotic neuronal state through addition of specific growth factors and whole-genome gene expression was examined throughout a time course of neuronal differentiation, demonstrating that a significant number of ASD candidate genes are coordinately regulated during the differentiation process.
Journal ArticleDOI

Application of weighted gene co-expression network analysis to identify key modules and hub genes in oral squamous cell carcinoma tumorigenesis.

TL;DR: The two modules and 10 hub genes identified provided references that will advance the understanding of mechanisms of tumorigenesis in OSCC and may serve as biomarkers and therapeutic targets for precise diagnosis and treatment of OSCC in the future.
Journal ArticleDOI

Discovery of core biotic stress responsive genes in Arabidopsis by weighted gene co-expression network analysis.

TL;DR: This work carried out a gene co-expression analysis of all currently publicly available microarray data, which were generated in experiments that studied the interaction of the model plant Arabidopsis thaliana with microbial pathogens to identify modules of functionally related co-expressed genes that are differentially expressed in response to multiple biotic stresses, and hub genes that may function as core regulators of disease responses.
Journal ArticleDOI

Neuronal CTGF/CCN2 negatively regulates myelination in a mouse model of tuberous sclerosis complex.

TL;DR: It is demonstrated that neuronal TSC1/2 orchestrates a program of oligodendrocyte maturation through the regulated secretion of connective tissue growth factor (CTGF) and that genetic deletion of CTGF from neurons mitigates the TSC-dependent hypomyelination phenotype.
References
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Journal ArticleDOI

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