Three statistical strategies were used to consider the covariates in the logistic models: (1) one including all the covariates listed in table 1; (2) one including the clinical comorbidity conditions only (hypertension, diabetes, AF, CHF, PAD, peptic ulcer, TIA and IHD); (3) one including the propensity score (calculated by predicting the probabilities of receiving low-dose aspirin ≥80%) only.
The sequence distribution, in terms of the degree of blockiness, in dual chemidomains of POB/PET copolyester is simulated from a model developed by us to predict the probability between block sequence and random sequence under a given composition and measuring condition.
After creating maps of the probability of occurrence of subtypes H3N2 and H5N1, we multiplied the maps by one another to predict the probability of co-occurrence of the 2 subtypes.
Then the probability calculations in Figure 1C are at odds with this by predicting that the highest probability sites for the interface are not in the hydrophobic binding patches.
As an example, for the digit 7 relative frequencies in the first 10 i, i = 0, 1, 2, 3, 4, 5, 6, 7 digits are 0, 0.095 0.097, 0.100250.09985, 0.1000207.1000207, which seem to be approaching 1 / 10 at rate predicted by the probability theory for random digits, i.e., a speed approximately proportional to 1 / n.
The likelihood of observing an event at a particular time is predicted by the probability density function (pdf).
Individuals were then grouped by predicted probability, and these groups were compared with the observed transfusions received.
Thus the performance on any individual letter/sound correspondence should be predicted by the probabilities of the letter location shown in Table 3.
In independent action it is assumed that the chemicals act independently via different mode of actions and the mixture effect is predicted by the probabilities of response of the individual chemicals.
Appropriate fit of logistic regression models was confirmed using the Hosmer Lemeshow goodness-of-fit test after grouping the data by predicted probabilities of deficiency into ten approximately equal-sized groups (Stata Base Reference Manual (K Q), Release 9. 2005.
