Volume 75, Issue 1 pp. 172-182
BIOMETRIC METHODOLOGY

Bayesian inference of hub nodes across multiple networks

Junghi Kim

Corresponding Author

Junghi Kim

Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.

email: [email protected]

email: [email protected]

email: [email protected]

email: [email protected]

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Kim-Anh Do

Corresponding Author

Kim-Anh Do

Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.

email: [email protected]

email: [email protected]

email: [email protected]

email: [email protected]

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Min Jin Ha

Corresponding Author

Min Jin Ha

Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.

email: [email protected]

email: [email protected]

email: [email protected]

email: [email protected]

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Christine B. Peterson

Corresponding Author

Christine B. Peterson

Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas, U.S.A.

email: [email protected]

email: [email protected]

email: [email protected]

email: [email protected]

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First published: 27 July 2018
Citations: 2

Summary

Hub nodes within biological networks play a pivotal role in determining phenotypes and disease outcomes. In the multiple network setting, we are interested in understanding network similarities and differences across different experimental conditions or subtypes of disease. The majority of proposed approaches for joint modeling of multiple networks focus on the sharing of edges across graphs. Rather than assuming the network similarities are driven by individual edges, we instead focus on the presence of common hub nodes, which are more likely to be preserved across settings. Specifically, we formulate a Bayesian approach to the problem of multiple network inference which allows direct inference on shared and differential hub nodes. The proposed method not only allows a more intuitive interpretation of the resulting networks and clearer guidance on potential targets for treatment, but also improves power for identifying the edges of highly connected nodes. Through simulations, we demonstrate the utility of our method and compare its performance to current popular methods that do not borrow information regarding hub nodes across networks. We illustrate the applicability of our method to inference of co-expression networks from The Cancer Genome Atlas ovarian carcinoma dataset.

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