Exact(1)
A separate analysis was applied in order to eliminate those trials with eye movement and eye blinks, during100ms before the sample onset up to 800ms after the test onset, by detecting those trials on which the peak-to-peak voltage in the horizontal and vertical eye movement channels exceeded 30 µV (<10% of trials).
Similar(59)
Baseline was corrected on the basis of activities, recorded 100ms before the sample stimulus onset.
Choice probability was calculated in an epoch before the onset of the stimulus (baseline epoch, −400 to −100 ms before sample onset), a post-sample epoch (200 1000 ms after sample onset) and in three divisions of the post-sample epoch (75 375 ms after sample onset, 375 675 ms after sample onset and 675 975 ms after sample onset).
In the course of each session drift correction was performed manually by the experimenter monitoring the eye tracker display using as a reference fixation period before sample onset.
Participants with no banked plasma sample from before the onset of the study period (preseason sample) or at the onset of clinical symptoms (acute sample) were excluded.
One sample was taken before the onset of treatment (T0 sample) and the second one was obtained when it was discontinued, 6 or 12 months later (T1 sample).
The EEG was rereferenced to the average reference and separated into epochs of 3700-ms duration for correct response trials only, starting 200 ms before the onset of the sample stimuli and ending 1000 ms after the onset of the test stimulus.
aMean and standard deviation of the intraocular distances were calculated on 12 samples acquired before the stimulus onset (t < 1.45 s).
Prospective studies are extremely important, since biomarkers can be discovered on samples collected years before the disease onset.
Serial sampling requires preplanning and good timing to establish cohorts with baseline blood samples before the epidemic's onset.
After the monkey acquired fixation, there was a variable delay (250 500 ms) before the onset of the sample image.
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