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As has been mentioned, we use QPSK modulation in our measurements.
An MPSK modulation in our simulation is defined as γ e (2n+1)π/M :n=0,1,…,M−1.
Distribution of relative modulation in our data set was bimodal, with a gap at 1.
Figure 12A shows the incidence of the different types of modulation in our V6A neuronal population.
Its modulation in our study partially resembles the N170 effects elicited by faces, but a delayed response, maybe caused by the delayed word presentation.
Peroxibase [ 44] reports 19 records of soybean peroxidases with homology to respiratory burst oxidases but none of them were found with a sign of expression modulation in our study.
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Modal interactions due to coupling have been studied which show the appearance of higher overtones as well as amplitude modulations in our theoretical model akin to the experimental observations.
The direction of sensory modulations in our study shows that the results reflect motor preparation, and not preparatory shifts of attention: attention typically enhances, rather than attenuates perception [17], [18].
Updating the semi-empirical model of cosmic rays (CR) modulation proposed in our previous work has been discussed.
The PDE is weak in Si and requires significant enhancement for practical modulation which in our case is enhanced via the FP resonator.
As a result, BPSK and QPSK are of particular interest and are used as the two main modulation constellations in our proposed adaptive scheme.
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