This value was obtained from the same 24 hours data set by taking the mean of all residuals irrespectively whether C N o values were large or not.
The data were separated into four 12 hour data sets, which correspond to the different light and dark periods and resulted in four 3-dimensional vectors for each gene and for each experiment.
The miRNA and mRNA expression profiles of paired samples were analyzed only in the 20 hour miRNA data set, as the number of significant miRNAs in the 4 hour dataset was too low to obtain reliable results.
After dropping the 644 individuals missing data on BMI, route type, or number of flying hours, the data set contained 15,683 records.
After the removal of elective admissions with a limited stay of less than 48 hours, the crude data set contained 5,859 feeding days.
In our model that was based on 5-minute and 1-hour EGF stimulation data set, contribution by ERK was masked by similar activation profile observed with EGFR.
However, the change in cell dispersal around 2 3 h of starvation, which is the basis for the SIRE walk, was not investigated by Potel and Mackay, and not mentioned by Li et al., who combined all observations during the entire starvation period from 0 to 10 hours into a single data set.
On a single Pentium processor CloseUp required more than one hour to run the simulated data set (1000 permutations for each CHS to get a reliable assessment), whereas CHSMiner took less than one minute.
This is clearly illustrated for propofol if one tries to extrapolate the compartmental model to times longer than those used in the experimental data set (10 hours).
Each plot was sampled for 15 or 30 min of each hour, producing a high-temporal resolution data set.
