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Harnessing Big Data for Systems Pharmacology.
Xie, Lei; Draizen, Eli J; Bourne, Philip E.
Afiliação
  • Xie L; Department of Computer Science, Hunter College, The City University of New York, New York, NY 10065; email: lei.xie@hunter.cuny.edu.
  • Draizen EJ; The Graduate Center, The City University of New York, New York, NY 10016.
  • Bourne PE; National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20894; email: philip.bourne@nih.gov.
Annu Rev Pharmacol Toxicol ; 57: 245-262, 2017 01 06.
Article em En | MEDLINE | ID: mdl-27814027
ABSTRACT
Systems pharmacology aims to holistically understand mechanisms of drug actions to support drug discovery and clinical practice. Systems pharmacology modeling (SPM) is data driven. It integrates an exponentially growing amount of data at multiple scales (genetic, molecular, cellular, organismal, and environmental). The goal of SPM is to develop mechanistic or predictive multiscale models that are interpretable and actionable. The current explosions in genomics and other omics data, as well as the tremendous advances in big data technologies, have already enabled biologists to generate novel hypotheses and gain new knowledge through computational models of genome-wide, heterogeneous, and dynamic data sets. More work is needed to interpret and predict a drug response phenotype, which is dependent on many known and unknown factors. To gain a comprehensive understanding of drug actions, SPM requires close collaborations between domain experts from diverse fields and integration of heterogeneous models from biophysics, mathematics, statistics, machine learning, and semantic webs. This creates challenges in model management, model integration, model translation, and knowledge integration. In this review, we discuss several emergent issues in SPM and potential solutions using big data technology and analytics. The concurrent development of high-throughput techniques, cloud computing, data science, and the semantic web will likely allow SPM to be findable, accessible, interoperable, reusable, reliable, interpretable, and actionable.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Farmacologia Clínica / Interpretação Estatística de Dados / Bases de Dados Factuais / Biologia de Sistemas Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Annu Rev Pharmacol Toxicol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Farmacologia Clínica / Interpretação Estatística de Dados / Bases de Dados Factuais / Biologia de Sistemas Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Annu Rev Pharmacol Toxicol Ano de publicação: 2017 Tipo de documento: Article