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Bayesian Hierarchical Varying-sparsity Regression Models with Application to Cancer Proteogenomics.
Ni, Yang; Stingo, Francesco C; Ha, Min Jin; Akbani, Rehan; Baladandayuthapani, Veerabhadran.
Afiliação
  • Ni Y; Department of Statistics and Data Sciences, The University of Texas at Austin.
  • Stingo FC; Department of Statistics, Computer Science, Applications "G. Parenti", The University of Florence.
  • Ha MJ; Department of Biostatistics, The University of Texas MD Anderson Cancer Center.
  • Akbani R; Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center.
  • Baladandayuthapani V; Department of Biostatistics, The University of Texas MD Anderson Cancer Center.
J Am Stat Assoc ; 114(525): 48-60, 2019.
Article em En | MEDLINE | ID: mdl-31178611
ABSTRACT
Identifying patient-specific prognostic biomarkers is of critical importance in developing personalized treatment for clinically and molecularly heterogeneous diseases such as cancer. In this article, we propose a novel regression framework, Bayesian hierarchical varying-sparsity regression (BEHAVIOR) models to select clinically relevant disease markers by integrating proteogenomic (proteomic+genomic) and clinical data. Our methods allow flexible modeling of protein-gene relationships as well as induces sparsity in both protein-gene and protein-survival relationships, to select ge-nomically driven prognostic protein markers at the patient-level. Simulation studies demonstrate the superior performance of BEHAVIOR against competing method in terms of both protein marker selection and survival prediction. We apply BEHAV-IOR to The Cancer Genome Atlas (TCGA) proteogenomic pan-cancer data and find several interesting prognostic proteins and pathways that are shared across multiple cancers and some that exclusively pertain to specific cancers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Am Stat Assoc Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: J Am Stat Assoc Ano de publicação: 2019 Tipo de documento: Article