Minimum information required for a DMET experiment reporting

Judit Kumuthini, Mamana Mbiyavanga, Emile R. Chimusa, Jyotishman Pathak, Panu Somervuo, Ron HN Van Schaik, Vita Dolzan, Clint Mizzi, Kusha Kalideen, Raj S. Ramesar, Milan Macek, George P. Patrinos, Alessio Squassina

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)1533-1545
Number of pages13
JournalPharmacogenomics
Volume17
Issue number14
DOIs
StatePublished - Sep 2016

Keywords

  • DMET
  • bioinformatics
  • minimum information requirement guidelines
  • personalized genomics
  • personalized medicine
  • pharmacogenomics
  • standardization

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Pharmacology

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