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Positive air-liquid biofilm samples were identify visually; the isolates were considered positive when a pellicle was covering the whole liquid surface.
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Samples were identified to species level.
Zones of inhibition surrounding samples were identified, photographed and measured in mm40.
For each region, samples were identified by textural grouping to create a number of sub-datasets.
Cells were cultured for 2 and 24 h, and the samples were identified as F2- 1-3) and F24- 1-3 F24- 1-3 F24- 1-3
The halophilic microorganisms from the environmental samples were identified by comparative phylogenetic analysis of their 16S rRNA gene sequences.
For processing, samples were identified by a number such that investigators were blind to the line and treatment associated with the sample.
As a result, previously characterized mutations from all control samples were identified in the first set of samples, regardless of the size of the pool.
In total, 97 genes with sequence variations detected in at least two RA samples but not in OA samples were identified.
The structure and chemical nature of the samples were identified by microscopic and spectroscopic techniques.
Four groups of samples were identified, which harbored Helicobacter as well as a diverse group of bacteria including Lactobacillus, Halomonas and Prevotella.
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