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With the measurement protocol outlined above, cross-contamination between consecutive samples is minimal, and data obtained from automatic measurements are indistinguishable from the data obtained by manual sampling (Supplementary Note 8).
where P(Vin) and P d V in d t are the power of the input signal and its derivation, respectively The time difference of between consecutive samples is quantized according to the precision T c timer.
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Finally, where the time between consecutive samples was varied, while good results were achieved at high sampling rates, increasing the sampling time was detrimental to the accuracy achieved.
Generally, the data found by FT-IR spectroscopy show a smoother trend/development over time than the respective reference data, where in some cases steep slopes, i.e., big differences between consecutive samples, were found.
The time difference between two consecutive samples is quantized instead of the time of each sample in order to prevent quantization error propagation.
Although agreement exists that a ≥ 4-fold increase in antibody titer between two consecutive samples is diagnostic, 4 such a diagnosis is retrospective and cannot guide initial treatment.
By letting the simulation progress between each two samples, two consecutive samples were not allowed to have the same closest "mate" to the examined organism.
A consecutive sample was used with 1429 cases between 2007 and 2014.
Consecutive sampling was used to recruit these participants.
Consecutive sampling was also used for qualitative data collection.
Consecutive sampling was used for quantitative data collection.
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