It can thus be expected that sampling variance will be lower for cereal-based retail items as opposed to whole grain.
It is expected that samples prepared from different precursors and different activation conditions will have distinct finger-prints.
It is expected that samples with greater values of K+/(Ca2+ + Mg2+) become more dispersed than those with lesser values.
It is expected that samples from TOA/OD and TOPO/OD will have modified surface states compared with that from pure OD.
However, it was expected that samples with differing PVLs and disease status would harbor varying numbers of sister cells, at least in their major clones.
Therefore, it is expected that sampling more broadly across the species range will increase the number of alleles detected.
It was expected that sample sizes, per analysis, using the RCT data (n = 996) would be excellent for evaluating construct validity, criterion validity and responsiveness of the Rasch-derived scalesare and Domescalesife scales.
In Tables 4, 5, 6, an asterisk is also marked where correlations were expected that were not found, and the sample sizes the analyses were performed on are included since in many cases there is an inadequate sample to detect a relationship.
It can be expected that these samples, with a high load of contaminants, also contain other POPs than the 13 organochlorine measured in this study, among which some are agonist or antagonist of the estrogen receptor, such as dioxins and furans [ 68].
For bacteria with larger genomes (2000 to 4000 ORFs) it can be expected that a sample from one biological situation, prepared and analysed by one procedure, will give access to about 10 50% of the proteins predicted by their genome [8, 9].
