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However, an even stronger predictor for the expected probability of misclassification should be an object's distance to the decision boundary of the classifier.
It thus appears improbable that misclassification should be responsible for the observed interactions.
The potential for misclassification should be considered.
However, such misclassification should be nondifferential with respect to BP and hypertension.
Any such misclassification should be non-differential with risk estimates biased towards the null.
Any misclassification should be nondifferential since pathologists were blinded to IGF-1 and IGFBP-3 levels, potentially attenuating our results.
Similar(40)
Without any distortion by the accompaniment, misclassification rates should be marginal.
Second, misclassification bias should be considered.
Then it could be suggested that, to prevent phenotypic misclassification, studies should be done on anti-CCP-negative subphenotypes.
Due to the possibility of misclassification, care should be taken when generalizing these results to the child level.
However, in case of any misclassification, it should be non-differential, thus should only cause an underestimation of the associations found.
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