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The median of the five MEPs at each of the five different stimulus levels, which were measured from peak to peak, were calculated and stored for analysis.
For statistical analysis, mean amplitude values within a time window from 160 to 200 ms (centred around the ERAN peak) were calculated for 4 Regions of Interest (ROIs; see also inset of Figure 3B): left anterior (AF3, F7, F3, FT7, FC3), right anterior (AF4, F8, F4, FT8, FC4), left posterior (T7, C3, CP5, P7, P3), and right posterior (T8, C4, CP6, P8, P4).
The chromatin and histone data for each peak were calculated as explained above.
The ratios of the second current peak to the first current peak were calculated and plotted relative to the recovery intervals.
The areas of each isotopic peak were calculated by their Gaussian distribution and then averaged to compare the relative abundance of each glycan between different samples.
Overall scores S1 and S2 for a given peak were calculated as the sum of individual scores s1 or s2 over all species.
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TL intensity for each glow peak was calculated by taking the area under dosimetric peak.
The particle size corresponding to this peak was calculated to be 6.7 nm.
The crystalline size at the (002) peak was calculated using the Scherrer formula [26 28].
The acidity of each peak was calculated according to the desorbed amount of NH3.
The average distance per peak is calculated by averaging all matched distances.
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