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For classification, all samples will be mapped onto one phylogenetic tree with the percentage of each sample on each level.
Individual sample on each chromosome.
The standard and the sample on each card were labeled.
The DGGE banding profiles for each sample were scored with the aid of Quantity One® fragment analysis software (Bio-Rad), where a single repeatedly run sample on each gel served as a reference marker.
All values were normalized to β-actin for the corresponding sample on each gel.
A standard curve was created for each assay by including serial dilutions of a reference sample on each plate.
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Ten plants were randomly sampled on each sampling day in July and September of 2006, and in May, July and September of 2007 and 2008.
To integrate over AC signals, the voltage was sampled on each refresh of the TV.
Assay quality was determined based on controls (DMSO-only samples) on each plate, as indexed by the Z' factor from Eq. (2)21,35.
The sample consisted of 122 first-year law students (55% male, mean age = 23.9 years), who collected five saliva samples on each of three consecutive days at each of five data collection waves.
Three trees per treatment were sampled on each occasion.
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