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Average fragment length and quantity after in vitro transcription using were assessed using an RNA Pico Kit on a 2100 Bioanalyzer (Agilent) according to the manufacturer's protocol.

Baseline weight (using digital scales with participants wearing light clothes and no shoes), height (assessed using a stadiometer) and blood pressure (an average of 3 measurements) were obtained at recruitment.

In the main French cereal areas, during a 6-week period in autumn 1999 2002, the proportion of viruliferous R. padi assessed using a TAS-ELISA technique was on average of 4.98% (range 2.01 9.91%).

The productivity of each population under the various conditions examined was assessed using a parameter calculated by multiplying the average height of the relevant transplants by their survival rate at the age of evaluation; this provides a measure of the population's overall fitness (Savolainen et al. 2007).

Connectivity combinations with statistically significant (p < 0.01) lag values were assessed using a two sample t-test of the difference between averaged HV and MO patient lags.

Adolescent recall of mobile telephone use was assessed using a self administered questionnaire which asked about number and average duration of calls per week.

The mean change from baseline in the monthly average number of migraine days were assessed using a mixed-effect model for repeated measures.

The changes in the average growth rate and period of oscillation are statistically significant, as assessed using a one-sided paired t-test (p<0.025).

Cell population purities were then assessed using a Cyan ADP flow cytometer (Becton Dickinson) with samples containing on average 95.31% CD3+CD4+ cells (range=90.21 98.78%) and 99.4% CD8+ cells (range=94.8 100%).

For this reason, lipid quantification was assessed by using an average of extinction coefficients for all fatty acids (Figure 3): y = 1.327 × 10- 2 x  +  2.911 × 10- 2 (R2 = 0.999), where y is the absorbance measured at 440 nm and x is the fatty acid concentration in milligrams per liter.

To identify vulnerabilities relevant to specific cancer subtypes, we conducted a large-scale RNAi screen in which viability effects of mRNA knockdown were assessed for 7,837 genes using an average of 20 shRNAs per gene in 398 cancer cell lines.