Literature DB >> 22256869

Semantically enabling pharmacogenomic data for the realization of personalized medicine.

Matthias Samwald1, Adrien Coulet, Iker Huerga, Robert L Powers, Joanne S Luciano, Robert R Freimuth, Frederick Whipple, Elgar Pichler, Eric Prud'hommeaux, Michel Dumontier, M Scott Marshall.   

Abstract

Understanding how each individual's genetics and physiology influences pharmaceutical response is crucial to the realization of personalized medicine and the discovery and validation of pharmacogenomic biomarkers is key to its success. However, integration of genotype and phenotype knowledge in medical information systems remains a critical challenge. The inability to easily and accurately integrate the results of biomolecular studies with patients' medical records and clinical reports prevents us from realizing the full potential of pharmacogenomic knowledge for both drug development and clinical practice. Herein, we describe approaches using Semantic Web technologies, in which pharmacogenomic knowledge relevant to drug development and medical decision support is represented in such a way that it can be efficiently accessed both by software and human experts. We suggest that this approach increases the utility of data, and that such computational technologies will become an essential part of personalized medicine, alongside diagnostics and pharmaceutical products.

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Year:  2012        PMID: 22256869      PMCID: PMC3957334          DOI: 10.2217/pgs.11.179

Source DB:  PubMed          Journal:  Pharmacogenomics        ISSN: 1462-2416            Impact factor:   2.533


  40 in total

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7.  Linked open drug data for pharmaceutical research and development.

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Journal:  Nat Biotechnol       Date:  2010-09-09       Impact factor: 54.908

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  6 in total

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2.  Pharmacogenomics in the pocket of every patient? A prototype based on quick response codes.

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3.  Electronic health record design and implementation for pharmacogenomics: a local perspective.

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4.  Search and visualization of gene-drug-disease interactions for pharmacogenomics and precision medicine research using GeneDive.

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5.  Making data on essential pharmacogenes available for every patient everywhere: the Medicine Safety Code initiative.

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  6 in total

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