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Exact(6)
To mimic spiking patterns of real biological neurons, one time step should correspond to approximately 0.5 ms of time.
In these simulations, each transmission from one node to an adjacent one requires 1 ms of time.
In this section, we study the response of (SNM) to harmonic input u_{n}= varphicos biggl(frac{omegapi n}{1000}+vartheta biggr), (6) with amplitude φ, phase shift (varthetain[0,2pi)), and where (omegain[0,1000]) corresponds to the input frequency in Hz assuming that one iteration of (SNM) corresponds to 0.5 ms of time.
Spectrograms were produced at 488 Hz of frequency resolution and 0.512 ms of time resolution.
Correspondingly, the spectrograms were produced at 488 Hz of frequency resolution and 0.512 ms of time resolution.
For experimental analysis, a single region of interest was drawn over the entire area within the barrier and plots with 120 ms of time integration over 1500 s were analysed.
Similar(54)
Given the temporal uncertainty (here ≈120 ms) of time-frequency-analysis techniques, it is possible that the cortical facilitation extends over a period of 400 ms, ranging from early perceptual analysis well into the P3 window (300 400 ms after stimulus onset).
The NMR spectra of initial and decomposed substrates were obtained by applying the following parameters: 13,000 Hz of rotor spin rate; 2 s of recycle time; 1H-power for CP 92.16 W: 1H 90° pulse 2.85 μs; 13C power for CP 150,4 W; 1 ms of contact time; 30 ms of acquisition time; 4000 scans.
The sequence parameters were 9.6 ms of repetition time (TR), 4.6 ms of echo time (TE), 1 mm thickness, and 256 m field of view (FOV).
MR images were acquired using a FLASH sequence with 1.43 ms of echo time (TE), 4.6 ms of repetition time (TR), and 17.5° of Gaussian excitation pulse.
The sequence parameters were 4,341 ms of repetition time (TR), 79.4 ms of echo time (TE), 1-mm thickness, and 256-mm field of view (FOV).
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