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(These are shown separately because the validation set was subjected to a more rigorous analysis of optimal placement).
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Three tissues (native fetal retina, native and cultured fetal choroid) were excluded from the validation set because of their physical proximity to RPE and the possibility of contamination by RPE.
Moreover, because 3 remaining sites were not sufficiently covered in the validation set to call somatic variants, these could not be evidence of the inaccuracy of whole-genome sequencing data, therefore not considered in the accuracy validation.
The interpolated coefficients are determined according to the validation set.
Subsequently, the revised CRI was evaluated in the validation set.
Identical patient profiles were found in the validation set.
In the validation set only adult data were used.
(C) Distribution of errors and predictions for the validation set.
Correlation coefficient for the validation set.
Because of the differences observed in the M/Z values of the peaks measured in the training and validation sets, we show in Table 2 the support-set used in the training set, along with the corresponding matching peaks used in the validation set.
The diagnostic performance was confirmed in the validation set.
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CEO of Professional Science Editing for Scientists @ prosciediting.com