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The proposed method assumes that the two microphone signals have similar content, in the sense that the microphones capture the same instruments with different weights (e.g., one microphone captures mostly the male voices of the chorus but the female voices are also present in the recording, and vice versa for the other microphone).
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However, in the same musical recording, the sound from the same source is played by the same player using the same instrument with typically the same playing style.
The ζ-potential was measured using the same instrument with the above-described conditions, except that the samples were diluted in 0.01 M KCl (9 1).
This gives us the opportunity to compare measurements performed over time with the same instrument with similar experimental strategies, as well as results obtained by the same technique at different synchrotrons, often involving dissimilar experimental strategies.
Purities were determined by flow cytometry analysis of the sorted cells on the same instrument with the same instrument settings.
Since it is relatively easy to play the modes on the same instrument with the same tuning, this property has both practical and theoretical appeal.
The CD133 studies were carried out using the same instrument, with antibodies from Miltenyi Biotec (Auburn, CA), according to the manufacturer instructions.
Demographic characteristics were assessed in the same instrument with simple questions.
The same instrument, with the same reliability and validity, produced highly different δ values in different populations, due to differences in distributions.
Degradation of FITC-casein (100 nM) was monitored using the same instrument with excitation at 490 nm and emission at 520 nm.
Most of the response variation we observed between the instruments, after conversion to Z-scores, was of the same magnitude as test retest on the same instrument with the same amplifier.
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CEO of Professional Science Editing for Scientists @ prosciediting.com