Abstract
Causal relationships between the vast numbers of bacterial species present in the human intestines contain a lot of potential information on the regulation of the gut in the healthy as well as in diseased states. Based on the hypothesis that the human gut microbiota constitutes a dynamic ecosystem, interesting correlations between the presences of the given species should exist at any time. In order to analyze this, we have developed GULDA, a cheap, flexible, reliable and high throughput qPCR-based gut low-density array (GULDA), which simultaneously gives the quantities of approximately 40 different selected bacterial 16S rRNA targets on all relevant phylogenetic levels in a given sample of DNA. In comparison to other strategies e.g. metagenomic sequencing and microarrays, GULDA focuses on selected targets only and requires only little complex bioinformactical post-processing.
Given the setup, where one standard qPCR program is used for ~40 primer sets, validation is important. We present here strategies involved in verification of GULDA as a valid tool for analysis of the human gut microbiota.
Given the setup, where one standard qPCR program is used for ~40 primer sets, validation is important. We present here strategies involved in verification of GULDA as a valid tool for analysis of the human gut microbiota.
Original language | English |
---|---|
Publication date | 2012 |
Number of pages | 1 |
Publication status | Published - 2012 |
Event | 7th Danish Conference on Biotechnology and Molecular Biology: Microbial Communities in Biotechnology, Health and Biomedicine - Hotel Munkebjerg, Vejle, Denmark Duration: 24 May 2012 → 25 May 2012 Conference number: 7 http://www.biokemi.org/meetings/67 |
Conference
Conference | 7th Danish Conference on Biotechnology and Molecular Biology |
---|---|
Number | 7 |
Location | Hotel Munkebjerg |
Country/Territory | Denmark |
City | Vejle |
Period | 24/05/2012 → 25/05/2012 |
Internet address |