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Dr. Gregory runs samples of speech through equipment that performs a kind of wave analysis known as fast Fourier transform analysis, which detects patterns in waves.
After the QCM-D runs, samples were rinsed with Millipore water, dried, and stored cool and dark.
After each spotting runs, samples of printed arrays were visualized with a fluorescent dye to control evenness of DNA deposition and spot morphology.
In all runs samples were taken at each cycle; two chains and the JTT substitution model [ 55] without ASRV were used.
Within runs, samples were assayed in triplicate with standard deviations of threshold cycle (CT) values not exceeding 0.5, and each q-PCR run was repeated at least twice.
In order to quantify fermentable sugars with the Aminex™ column during fermentation runs, samples that contained sucrose had to be pre-treated with invertase before column chromatography.
Similar(53)
Bayesian inference analyses were performed with MrBayes v351 using two parallel runs, sampling every 100 generations.
The analyses were conducted using two million generations in two independent runs, sampling trees every 100 generations.
Four chains were run simultaneously for 2 million generations in two independent runs, sampling trees every 100 generations.
BD fluorosphere counting beads were added to cocktails before running samples.
The possibility to run samples in batch, and the special arrangement developed for this is described.
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