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Reaction specificity was evaluated using PCR amplification curves along with specific melting temperatures of probes on DNA extracted from 13 Mycobacterium species.
Assay specificity was evaluated by eliminating InO coating of wells.
Primer specificity was evaluated in silico by BLAST analysis and agarose gel electrophoresis.
The limit of detection of each target, as well as specificity, was evaluated.
Method specificity was evaluated analysing 40 different tissues (mammalians, avian, fish) and flour samples.
The analytical specificity was evaluated on a collection of 68 clinically relevant, phylogenetically related or serologically cross-reacting micro-organisms.
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The sensitivity and specificity were evaluated using Monte Carlo simulations.
The specificity is evaluated by distinguishing target L. monocytogenes from other bacteria.
In the present work, two protocols of real-time qPCR based on SYBR Green and TaqMan were developed, and their sensitivity and specificity were evaluated.
In the present work, two protocols of real-time PCR (qPCR) based on SYBR Green and TaqMan were developed, and their sensitivity and specificity were evaluated.
A SimpleProbe® real-time PCR assay was designed to detect the single nucleotide polymorphism at nucleotide 363 in CYTb gene of B. gibsoni and the sensitivity and specificity were evaluated by comparing the results from the conventional DNA sequencing method.
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specificity was estimated
specification was evaluated
characteristic was evaluated
distinctiveness was evaluated
specificity was assessed
specificity was validated
clarity was evaluated
accuracy was evaluated
specificity was ascertained
precision was evaluated
diversity was evaluated
characteristics was evaluated
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