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Missing values (proteins not identified in the sample) were replaced with 0.5 of the minimum protein expression value [ 79].
The control and standard were subjected to the same procedure except for the control, where there was no addition of sample and for the standard 1 mL of sample were replaced with 1 mg of PG, BHT, and BHA.
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For the positive control, sample was replaced with ascorbic acid.
In this study, each sample was replaced with the median value of a window covering three pre- and post-samples.
The investigations show that the native oxide on the sample is replaced by self assembled nanotube array by anodization.
The positive and negative controls were subjected to the same procedures as the sample, except that for the negative control, only the solvent was added, and for the positive control, sample was replaced with ascorbic acid.
Then the sample was replaced in the acid condensation again, where the corrosion was accelerated because the acid could easily go through the cracks and corrode the substrate underneath.
We follow the random update introduced in [17] and adopted in [19] and [20], where a randomly chosen sample is replaced by the new value, as this extends the time window spanned by the model.
The need for making unique primer combinations for each sample is replaced by having the same 96 position specific primer pairs for all PCR plates.
One fourth of the sample is replaced every year.
In blank, the media sample was replaced with de-ionized (DI) water.
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