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Calibration analysis for SMART models developed from baseline plus serial data are shown in Table 6.
Serial data are shown in figure 2 and 3. Figure 2 shows plasma levels of the smaller proteins CC16 and sRAGE, figure 3 shows plasma levels of the larger proteins SP-D and KL-6.
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The serial data is converted into parallel streams by the serial-to-parallel (S/P) conversion block.
In addition, serial data were unavailable for blood cholesterol, triglyceride, and glucose concentrations that are influenced by capecitabine.
To study changes over time in control patients and patients developing VAP, serial data were analyzed using linear mixed models.
Serial data were evaluated with respect to renal function, cardiac mass, pain, quality of life, and tolerability/safety.
Serial data were then summarised for each individual by recording the average WHIM hierarchical scores within each month of the programme (up to 6 months).
Serial data were compared within and between groups by repeated measures analysis of variance, with a 'between groups' and a 'repeated measures' comparison.
The relationship between the EF score and serial data was analyzed using Pearson's correlation coefficient, and that between the EF score and discrete variable data was analyzed using Spearman's rank correlation coefficient.
Through B/R conversion, according to (4), the serial data streams are divided into V parallel residue subchannels transmitting signals, which are represented as (8) in the RNS.
Finally, serial digital data is converted to analog data by using D/A block.
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