Network-based cancer heterogeneity analysis incorporating multi-view of prior information

Author:

Li Yang1ORCID,Xu Shaodong1,Ma Shuangge2ORCID,Wu Mengyun3ORCID

Affiliation:

1. Center for Applied Statistics, School of Statistics, Statistical Consulting Center, and RSS and China-Re Life Joint Lab on Public Health and Risk Management, Renmin University of China, Beijing 100872, China

2. Department of Biostatistics, Yale School of Public Health , New Haven, CT 06520, USA

3. School of Statistics and Management, Shanghai University of Finance and Economics , Shanghai 200433, China

Abstract

Abstract Motivation Cancer genetic heterogeneity analysis has critical implications for tumour classification, response to therapy and choice of biomarkers to guide personalized cancer medicine. However, existing heterogeneity analysis based solely on molecular profiling data usually suffers from a lack of information and has limited effectiveness. Many biomedical and life sciences databases have accumulated a substantial volume of meaningful biological information. They can provide additional information beyond molecular profiling data, yet pose challenges arising from potential noise and uncertainty. Results In this study, we aim to develop a more effective heterogeneity analysis method with the help of prior information. A network-based penalization technique is proposed to innovatively incorporate a multi-view of prior information from multiple databases, which accommodates heterogeneity attributed to both differential genes and gene relationships. To account for the fact that the prior information might not be fully credible, we propose a weighted strategy, where the weight is determined dependent on the data and can ensure that the present model is not excessively disturbed by incorrect information. Simulation and analysis of The Cancer Genome Atlas glioblastoma multiforme data demonstrate the practical applicability of the proposed method. Availability and implementation R code implementing the proposed method is available at https://github.com/mengyunwu2020/PECM. The data that support the findings in this paper are openly available in TCGA (The Cancer Genome Atlas) at https://portal.gdc.cancer.gov/. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

National Natural Science Foundation of China

Shanghai Research Center for Data Science and Decision Technology

National Institutes of Health

Platform of Public Health & Disease Control and Prevention

Major Innovation & Planning Interdisciplinary Platform for the ‘Double-First Class’ Initiative

Renmin University of China

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

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