Sentence examples for stimulus trials from inspiring English sources

First, it suggests that a much smaller number of stimulus trials is needed for perfect identification.

3.2, we consider here the identification of low-rank DSP of complex cells from spike times generated when multiple stimulus trials are presented.

Low-rank functional identification reaches nearly machine precision with about 746 spikes, which corresponds to about 70 stimulus trials (see also Figure 14).

Figure 3 shows the PDFs of four example ISIs, i.e., for four different histories of past spikes, calculated by the four numerical methods, first Volterra, second Volterra, Fokker Planck PDF and Fokker Planck CDF, under single stimulus trials.

Theorems 5 and 6 suggest that decoding of spatio-temporal stimuli encoded by a population of complex cells is dual to the functional identification of the DSP of complex cells presented with multiple stimulus trials.

We show that the responses in both tails of our empirical RT distributions on stimulus trials are indeed correctly predicted by the race model and can be considered false alarms.

While analogous to the single-stimulus rating, in double-stimulus trials a reference photo and a test photo are presented in random order, one after another, for a fixed presentation time (e.g., 3 s); Forced-Choice.

Third, to measure prepulse-elicited reactivity we included data from prepulse-alone and no-stimulus trials.

All PPI test sessions consisted of startle trials (PULSE-ALONE), prepulse trials (PREPULSE+PULSE), and no-stimulus trials (NOSTIM).

Blank no-stimulus trials were intermixed randomly.

The peak of EPSC2 was determined by subtracting a peak-scaled EPSC from interleaved single-stimulus trials (see Fig.  4 A).