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The digital MIQE guidelines: Minimum information for publication of quantitative digital PCR experiments

  • Jim F. Huggett
  • , Carole A. Foy
  • , Vladimir Benes
  • , Kerry Emslie
  • , Jeremy A. Garson
  • , Ross Haynes
  • , Jan Hellemans
  • , Mikael Kubista
  • , Reinhold D. Mueller
  • , Tania Nolan
  • , Michael W. Pfaffl
  • , Gregory L. Shipley
  • , Jo Vandesompele
  • , Carl T. Wittwer
  • , Stephen A. Bustin
  • LGC Ltd.
  • Genomics Core Facility
  • National Measurement Institute, Australia
  • University College London
  • National Institute of Standards and Technology
  • Ghent University Hospital
  • Institute of Biotechnology of the Czech Academy of Sciences
  • Sequenom, Inc.
  • Sigma Custom Products
  • Shipley Consulting
  • University of Utah School of Medicine
  • Anglia Ruskin University

Research output: Contribution to journalArticlepeer-review

753 Scopus citations

Abstract

There is growing interest in digital PCR (dPCR) because technological progress makes it a practical and increasingly affordable technology. dPCR allows the precise quantification of nucleic acids, facilitating the measurement of small percentage differences and quantification of rare variants. dPCR may also be more reproducible and less susceptible to inhibition than quantitative real-time PCR (qPCR). Consequently, dPCR has the potential to have a substantial impact on research as well as diagnostic applications. However, as with qPCR, the ability to perform robust meaningful experiments requires careful design and adequate controls. To assist independent evaluation of experimental data, comprehensive disclosure of all relevant experimental details is required. To facilitate this process we present the Minimum Information for Publication of Quantitative Digital PCR Experiments guidelines. This report addresses known requirements for dPCR that have already been identified during this early stage of its development and commercial implementation. Adoption of these guidelines by the scientific community will help to standardize experimental protocols, maximize efficient utilization of resources, and enhance the impact of this promising new technology.

Original languageEnglish
Pages (from-to)892-902
Number of pages11
JournalClinical Chemistry
Volume59
Issue number6
DOIs
StatePublished - Jun 2013

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