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The holdout estimator is based on splitting the data in two random non-overlapping parts, deriving a signature from the first one and assessing its error in the second one.
Analyses were conducted in two random half-samples.
Cells in two random wells were counted daily using a hematocytometer.
The sequencing reactions were carried out in two random nasal mucosa samples with forward and reverse primers in separate reactions.
Data were obtained from four or five plants for each accession (INRA and Clark sets, respectively), simultaneously grown in two random blocks.
In order to cross-validate factor models, the initial sample (n = 6,506) was divided in two random subsamples of the same size (n = 3,253).
Similar(48)
The positively stained cells in the sections were counted in five random fields per section and three sections per kidney.
We then counted bacterial cells in ten random fields from each subsample beneath an epifluorescent microscope to derive bacterial densities.
Images were taken at ×100 magnification and the number of colonies was quantified by counting in five random fields.
In three random columns by each critic, Lane uses six semicolons in two columns and four in one; Denby weighs in at four, three, and two.
Percent of phagocytizing cells was calculated in eight random fields of view using the following equation: = [(number of macrophages with engulfed bioparticles)/ total number of macrophages)] × 100.
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