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Raw data were sampled by IDEEQ every 2 ms, averaged and stored to disc every cardiac cycle.
All hemodynamic and cardiodynamic data were sampled by a laboratory computer at 1000 Hz, and mean values for 10 cardiac cycles were saved on the laboratory computer for future analysis.
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Days on which data were sampled were defined by the study coordinator and equally distributed across weekdays.
The trackball data were sampled online at 10 kHz, controlled by custom-programmed software.
Data was sampled every 1 ms by a recording system controlled by a GPS-calibrated clock.
To compute this reduction, the expected statistics of unknown data to be sampled by different candidate sampling behaviors are assimilated.
Sequences of the HIV-1 data set were sampled from the data set used by Penn et al. (2008).
These data were re-sampled by bilinear and cubic interpolation (area of 312 and 312 μm and 1.5 mm thickness, continuous sections) for the final three-dimensional rendering.
The data is re-sampled by bilinear and cubic interpolation for the final 3D rendering.
The data are listed sample-by-sample in order of clinical progression beginning with prostatic intraepithelial neoplasia ('PIN') cases and progressing to localised prostate cancer ('Primary Carcinoma'), followed by metastatic hormone naïve cases and finally metastatic hormone refractory samples.
These data were then re-sampled by bilinear and cubic interpolation for the final three-dimensional rendering.
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