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The region giving y=−1 more likely than not tends to be more separated, and it is difficult to get any sample from a number of separated regions at the first random sampling.
We tested 22 healthy subjects, enabling assessment of imaging results at a second (random effects) level of analysis.
At the second stage, after random variables outcomes become known, correction actions must be taken, which have a cost.
At the second level, voxelwise random effects models were used to examine task-related and performance-related activation.
At the second stage, a random sample of households was selected based on a sampling frame from the 1994 census and adapted for recent population changes.
Effects of interest were then assessed at the second level in a random effects analysis.
The absence of overlap in genetic similarity at the second peak between the random subsets and reassorted data provides evidence to support this claim.
At the second level of the random effects analysis, we split the subjects into two groups; left TLE and right TLE.
At the second level of the random effects analysis, we divided the subjects into three groups: healthy volunteers, left temporal lobe epilepsy and right temporal lobe epilepsy patients.
At the second level of the random effects analysis, we divided the subjects into three groups: Healthy volunteers, left TLE, and right TLE patients.
At the second level of the random effects analysis, subjects were divided into two groups, patients with left and right TLE.
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