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The sensitivity/specificity trade-off is readily seen in this figure, although the entire range cannot be explored for all methods using standard parameters.
We describe a new method of non-overlapping oligonucleotide frequency ranges for species identification and compare its species resolution ability with p-distance, Euclidean distance (derived from oligonucleotide frequency) and nucleotide character based methods, using standard barcode loci.
Native crystals were obtained using the hanging (AfChiA1) and sitting drop (ScCTS1) vapour diffusion methods using standard protocols [23,25].
The existing methods, using standard radiographs, showed a significantly lower visibility, especially regarding the use of the hamstring graft.
We evaluated these methods using standard TGE metrics and determined the ability to identify several classes of genetic mutations in three sets of 96 samples, including 48 controls.
The antibiotic susceptibility was identified by routine diagnostic methods using standard disk diffusion for Gram-positive and Gram-negative (MultiBac I.D., México D.F).
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Relaxation methods used standard procedures (Barbato et al., 1992; Ferrage et al., 2006, 2009, 2010).
Neither of these methods uses standard qualitative research methodology, but instead combines qualitative and epidemiologic approaches.
The two methods use standard algorithms (greedy [ 9] and Markov chain Monte Carlo (MCMC) [ 11]) to find the set of processes with the greatest fit to the observed data.
For each of the methods used (standard, tip, and hemisphere), we had 20 double sets of radiographs on which to calculate precision.
Alkalinity was determined by titrimetric method using standard 0.02 N H2SO4.
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