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Meta-analysis of Inter-species Liver Co-expression Networks Elucidates Traits Associated with Common Human Diseases

Overview of attention for article published in PLoS Computational Biology, December 2009
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Title
Meta-analysis of Inter-species Liver Co-expression Networks Elucidates Traits Associated with Common Human Diseases
Published in
PLoS Computational Biology, December 2009
DOI 10.1371/journal.pcbi.1000616
Pubmed ID
Authors

Kai Wang, Manikandan Narayanan, Hua Zhong, Martin Tompa, Eric E. Schadt, Jun Zhu

Abstract

Co-expression networks are routinely used to study human diseases like obesity and diabetes. Systematic comparison of these networks between species has the potential to elucidate common mechanisms that are conserved between human and rodent species, as well as those that are species-specific characterizing evolutionary plasticity. We developed a semi-parametric meta-analysis approach for combining gene-gene co-expression relationships across expression profile datasets from multiple species. The simulation results showed that the semi-parametric method is robust against noise. When applied to human, mouse, and rat liver co-expression networks, our method out-performed existing methods in identifying gene pairs with coherent biological functions. We identified a network conserved across species that highlighted cell-cell signaling, cell-adhesion and sterol biosynthesis as main biological processes represented in genome-wide association study candidate gene sets for blood lipid levels. We further developed a heterogeneity statistic to test for network differences among multiple datasets, and demonstrated that genes with species-specific interactions tend to be under positive selection throughout evolution. Finally, we identified a human-specific sub-network regulated by RXRG, which has been validated to play a different role in hyperlipidemia and Type 2 diabetes between human and mouse. Taken together, our approach represents a novel step forward in integrating gene co-expression networks from multiple large scale datasets to leverage not only common information but also differences that are dataset-specific.

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The data shown below were compiled from readership statistics for 111 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 9 8%
Germany 3 3%
Colombia 1 <1%
Argentina 1 <1%
Netherlands 1 <1%
Japan 1 <1%
Belgium 1 <1%
Unknown 94 85%

Demographic breakdown

Readers by professional status Count As %
Researcher 34 31%
Student > Ph. D. Student 26 23%
Professor > Associate Professor 11 10%
Other 8 7%
Student > Master 8 7%
Other 18 16%
Unknown 6 5%
Readers by discipline Count As %
Agricultural and Biological Sciences 64 58%
Computer Science 14 13%
Medicine and Dentistry 12 11%
Biochemistry, Genetics and Molecular Biology 9 8%
Social Sciences 1 <1%
Other 1 <1%
Unknown 10 9%