Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/132969
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Type: Journal article
Title: pDriver: a novel method for unravelling personalized coding and miRNA cancer drivers
Author: Pham, V.V.H.
Liu, L.
Bracken, C.P.
Nguyen, T.
Goodall, G.J.
Li, J.
Le, T.D.
Citation: Bioinformatics, 2021; 37(19):3285-3292
Publisher: Oxford University Press (OUP)
Issue Date: 2021
ISSN: 1367-4803
1460-2059
Editor: Gorodkin, J.
Statement of
Responsibility: 
Vu V.H. Pham, Lin Liu, Cameron P. Bracken, Thin Nguyen, Gregory J. Goodall, Jiuyong Li and Thuc D. Le
Abstract: Motivation: Unravelling cancer driver genes is important in cancer research. Although computational methods have been developed to identify cancer drivers, most of them detect cancer drivers at population level. However, two patients who have the same cancer type and receive the same treatment may have different outcomes because each patient has a different genome and their disease might be driven by different driver genes. Therefore new methods are being developed for discovering cancer drivers at individual level, but existing personalized methods only focus on coding drivers while microRNAs (miRNAs) have been shown to drive cancer progression as well. Thus, novel methods are required to discover both coding and miRNA cancer drivers at individual level. Results: We propose the novel method, pDriver, to discover personalized cancer drivers. pDriver includes two stages: (i) constructing gene networks for each cancer patient and (ii) discovering cancer drivers for each patient based on the constructed gene networks. To demonstrate the effectiveness of pDriver, we have applied it to five TCGA cancer datasets and compared it with the state-of-the-art methods. The result indicates that pDriver is more effective than other methods. Furthermore, pDriver can also detect miRNA cancer drivers and most of them have been confirmed to be associated with cancer by literature. We further analyze the predicted personalized drivers for breast cancer patients and the result shows that they are significantly enriched in many GO processes and KEGG pathways involved in breast cancer. Availability and implementation: pDriver is available at https://github.com/pvvhoang/pDriver.
Rights: © The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com
DOI: 10.1093/bioinformatics/btab262
Grant ID: http://purl.org/au-research/grants/arc/DE200100200
http://purl.org/au-research/grants/arc/DP170101306
Published version: http://dx.doi.org/10.1093/bioinformatics/btab262
Appears in Collections:Medicine publications

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