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Minimum information required for a DMET experiment reporting
J. Kumuthini, M. Mbiyavanga, ER. Chimusa, J. Pathak, P. Somervuo, RH. Van Schaik, V. Dolzan, C. Mizzi, K. Kalideen, RS. Ramesar, M. Macek, GP. Patrinos, A. Squassina,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
NLK
ProQuest Central
od 2000-02-01 do 2020-12-31
Health & Medicine (ProQuest)
od 2000-02-01 do 2020-12-31
PubMed
27548815
DOI
10.2217/pgs-2016-0015
Knihovny.cz E-zdroje
- MeSH
- farmakogenetika * MeSH
- interpretace statistických dat MeSH
- lidé MeSH
- šíření informací MeSH
- výzkumný projekt * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
AIM: To provide pharmacogenomics reporting guidelines, the information and tools required for reporting to public omic databases. MATERIAL & METHODS: For effective DMET data interpretation, sharing, interoperability, reproducibility and reporting, we propose the Minimum Information required for a DMET Experiment (MIDE) reporting. RESULTS: MIDE provides reporting guidelines and describes the information required for reporting, data storage and data sharing in the form of XML. CONCLUSION: The MIDE guidelines will benefit the scientific community with pharmacogenomics experiments, including reporting pharmacogenomics data from other technology platforms, with the tools that will ease and automate the generation of such reports using the standardized MIDE XML schema, facilitating the sharing, dissemination, reanalysis of datasets through accessible and transparent pharmacogenomics data reporting.
Centre for Proteomic and Genomic Research Cape Town South Africa
Institute of Biotechnology University of Helsinki Helsinki Finland
Citace poskytuje Crossref.org
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- $a AIM: To provide pharmacogenomics reporting guidelines, the information and tools required for reporting to public omic databases. MATERIAL & METHODS: For effective DMET data interpretation, sharing, interoperability, reproducibility and reporting, we propose the Minimum Information required for a DMET Experiment (MIDE) reporting. RESULTS: MIDE provides reporting guidelines and describes the information required for reporting, data storage and data sharing in the form of XML. CONCLUSION: The MIDE guidelines will benefit the scientific community with pharmacogenomics experiments, including reporting pharmacogenomics data from other technology platforms, with the tools that will ease and automate the generation of such reports using the standardized MIDE XML schema, facilitating the sharing, dissemination, reanalysis of datasets through accessible and transparent pharmacogenomics data reporting.
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- $a Mbiyavanga, Mamana $u Centre for Proteomic & Genomic Research, Cape Town, South Africa.
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- $a Chimusa, Emile R $u Centre for Proteomic & Genomic Research, Cape Town, South Africa. Computational Biology Group, Institute for Infectious Diseases & Molecular Medicine, University of Cape Town, South Africa.
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- $a Pathak, Jyotishman $u Division of Biomedical Statistics & Informatics, Department of Health Sciences Research, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
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- $a Somervuo, Panu $u Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
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- $a Van Schaik, Ron Hn $u Department of Clinical Chemistry, Erasmus University Medical Center Rotterdam, Room Na-415, Wytemaweg 80, 3015CN Rotterdam, The Netherlands.
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- $a Mizzi, Clint $u Department of Bioinformatics, Faculty of Medicine & Health Sciences, Erasmus University Medical Center, Rotterdam, The Netherlands. Department of Physiology & Biochemistry, Faculty of Medicine and Surgery, University of Malta, Malta.
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- $a Kalideen, Kusha $u UCT/SA MRC Human Genetics Research Unit, Division of Human Genetics, Institute for Infectious Diseases & Molecular Medicine, Division of Human Genetics, University of Cape Town, South Africa.
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- $a Macek, Milan $u Department of Biology & Medical Genetics, Charles University Prague & 2nd Faculty of Medicine, Prague, Czechia.
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- $a Patrinos, George P $u Department of Bioinformatics, Faculty of Medicine & Health Sciences, Erasmus University Medical Center, Rotterdam, The Netherlands. Department of Pharmacy, School of Health Sciences, University of Patras, Patras, Greece.
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- $a Squassina, Alessio $u Laboratory of Pharmacogenomics, Section of Neuroscience & Clinical Pharmacology, Department of Biomedical Sciences, University of Cagliari, sp 8 Sestu-Monserrato, Km 0.700, 09042 Cagliari, Italy.
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