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The same region of the tissue was used for all animals to minimize sampling variation that resulted from differences in cell size and anatomical location.
Values of the variance components used in the simulation were assumed known to minimize sampling variation.
Sampled shoots were carefully selected so that they were as similar to each other as possible in size and shape to minimize sampling variation.
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To minimize sample variation, we used high quality RNA.
To minimize sample variations, β-actin was used as the reference gene.
To minimize sample variations, mRNA expression of the target gene was normalized relative to the expression of the housekeeping gene actin.
Attention to sample preparation, particularly the use of small increments to minimize sample density variation, gives a marked reduction in error bars allowing processes to be clearly observed.
Although samples were not processed simultaneously, aliquoted and frozen reagents were used for DNA extractions and PCR amplifications in order to minimize sample-to-sample variation.
Be consistent with all the samples collected, to minimize sample-to-sample variation in the amount of tissue pooled.
The assays use exogenous ATIII to minimize sample-to-sample variation, which allows the heparin level to be the primary variable in the assay.
The controls had been prepared in parallel using the same exome capture kits and on the same flow cell to minimize sample-to-sample variation.
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