Abstract

BackgroundIdentifying gene regulatory network (GRN) from time course gene expression data has attracted more and more attentions. Due to the computational complexity, most approaches for GRN reconstruction are limited on a small number of genes and low connectivity of the underlying networks. These approaches can only identify a single network for a given set of genes. However, for a large-scale gene network, there might exist multiple potential sub-networks, in which genes are only functionally related to others in the sub-networks.ResultsWe propose the network and community identification (NCI) method for identifying multiple subnetworks from gene expression data by incorporating community structure information into GRN inference. The proposed algorithm iteratively solves two optimization problems, and can promisingly be applied to large-scale GRNs. Furthermore, we present the efficient Block PCA method for searching communities in GRNs.ConclusionsThe NCI method is effective in identifying multiple subnetworks in a large-scale GRN. With the splitting algorithm, the Block PCA method shows a promosing attempt for exploring communities in a large-scale GRN.

Highlights

  • Identifying gene regulatory network (GRN) from time course gene expression data has attracted more and more attentions

  • To accomodate the large-scale GRN inference, we propose a block principal component analysis (Block PCA) method, which explores community structure information for the network and community identification (NCI) method

  • We examine the NCI method based on two synthetic gene regulatory networks with different sizes

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Summary

Results

We propose the network and community identification (NCI) method for identifying multiple subnetworks from gene expression data by incorporating community structure information into GRN inference. We present the efficient Block PCA method for searching communities in GRNs

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Newman M
15. Newman M
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