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A sequence mismatch was recorded only once for each EST library.
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The position and base transition of the indicated mismatches are recorded in an additional set of score files.
Mismatch negativity was recorded for spectral as well as temporal contrasts using speech and tonal stimuli.
The BLAST algorithm was used to find the homologs of each anchor in the target genome T. The mismatch score for each anchor was recorded and a normalized score was computed as described in Methods (Fig S1).
The number of volumes with registration mismatch vector equal to zero (no registration required) was recorded per group.
In an oddball task designed to elicit mismatch negativity (MMN), subjects ignored these stimuli while their brain activity was recorded.
Electrophysiologically measured mismatch responses were recorded to changes in consonants as participants passively listened to a repeating four syllable CV-string.
Since the mismatch response is recorded very early after auditory input and neither articulation or vocabulary knowledge play any role in the task, our paradigm thus permitted us to assess the degree to which such external factors determine individual differences in nonword repetition.
Auditory negative difference (Nd) and mismatch negativity (MMN) were recorded in a tonal dichotic listening task.
The observed mismatches between patient and donor were recorded by position number and the two different amino acids.
Auditory and visual deviant stimuli evoke mismatch negativity (MMN) responses, which can be recorded with electroencephalography (EEG) and magnetoencephalography (MEG).
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