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The importance of the sample in determining the fraction of gene families that have been impacted by mobile elements is unclear, but one might suspect that the number of gene families showing such impact might increase as we explore other wise of identifying sequences that have been impacted by LGT.
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Mean temporal variation was less for samples taken on a daily basis than mean temporal variation for samples taken every 5 days (P<0.02), indicating the importance of the temporal scale of sampling in determining community constancy.
Furthermore, changes in sampling conditions, such as ambient temperature and wind speed, may have also introduced bias into our sampling in determining concentrations of breath metabolites, especially for volatile compounds.
Our study was limited by sample size in determining the relationship of adiponectin and prior MACE burden.
These studies indicate the importance of the sampling method in determining tear glucose concentrations.
Scale of sampling is important in determining spatial autocorrelation in clonal species [54].
The numerical examples show that JA is very accurate in determining sample sizes.
The concentration of MDA in sample was determined in nmol/ml (Ohkawa et al., 1979).
The number of viable cells in each sample was determined in triplicate using the CellTiter 96 AQueous Non-Radioactive Cell Promegaration Assay (MTS assay) (Promega).
From January 2003 through December 2004, MICs of antifungal drugs with respect to strains of Candida in samples were determined in an external microbiology laboratory that was affiliated with the University.
Relaxed density, RD, of the sample was determined in accordance to international standard ISO 3131.
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