The use of propidium monoazide in conjunction with qPCR and Illumina sequencing to identify and quantify live yeasts and bacteria
- 1 October 2016
- journal article
- Published by Elsevier in International Journal of Food Microbiology
- Vol. 234, 53-59
Abstract
No abstract availableKeywords
Funding Information
- UBC Okanagan Biology Department
- BC Wine Grape Council (AIP-PO10-BCWGC, 2014)
- NSERC (CRDPJ-406796-10, 2011)
This publication has 22 references indexed in Scilit:
- Monitoring Seasonal Changes in Winery-Resident MicrobiotaPLOS ONE, 2013
- Defining the core Arabidopsis thaliana root microbiomeNature, 2012
- Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platformsThe ISME Journal, 2012
- A tale of three next generation sequencing platforms: comparison of Ion torrent, pacific biosciences and illumina MiSeq sequencersBMC Genomics, 2012
- Global patterns of 16S rRNA diversity at a depth of millions of sequences per sampleProceedings of the National Academy of Sciences, 2010
- Quantitative Approach to Determining the Contribution of Viable-but-Nonculturable Subpopulations to Malolactic Fermentation ProcessesApplied and Environmental Microbiology, 2009
- Discrimination of Viable and Dead Fecal Bacteroidales Bacteria by Quantitative PCR with Propidium MonoazideApplied and Environmental Microbiology, 2009
- The MIQE Guidelines: Minimum Information for Publication of Quantitative Real-Time PCR ExperimentsClinical Chemistry, 2009
- Selective detection of live bacteria combining propidium monoazide sample treatment with microarray technologyJournal of Microbiological Methods, 2009
- Real-Time Quantitative PCR (QPCR) and Reverse Transcription-QPCR for Detection and Enumeration of Total Yeasts in WineApplied and Environmental Microbiology, 2006