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Our LOAD system capable of bacterial identification of Mycobacterium tuberculosis (TB) and Acinetobacter baumanii (Ab) with the detection limits 103 cfu/mL TB in sputum and 102 cfu/mL Ab in blood within 2 h after sample loading.
Bacterial identification of the nine selected isolates was based on 16S rDNA sequence analysis.
Bacterial identification of the strain was performed by 16S rRNA sequencing.
It was not necessary to have conclusive bacterial identification of the psoas drainage fluid, since previous antibiotic use could have given a false-negative result.
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The 2013 updates increased the number of bacterial identifications to 174,853 and the number of monitored bacterial species to 611 (43 new bacterial species were added).
The bacterial identification capability of our multiplex PCR is comparable to that of the conventional blood culture approach, especially in some patient biopsies.
The clinician will record number of colonies, the colour of colonies for bacterial identification and the antibiotic resistance of the pure or predominant.
Compared to conventional methods of bacterial identification, the FISH method produced positive results for > 90% of the samples tested.
In case of discrepancies between the two methods the results of bacterial identification were confirmed by ID32 Staph or Rapid ID32 Strep.
It was also considered as a precise method of bacterial identification because it can provide bacterium species-specific signature (Clarridge 2004; Preveena and Bhore 2013).
To maximize the accuracy of bacterial identification, we rigorously screened sequences to remove poor quality reads.
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