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Table 5 shows that application of these weights affects only slightly the results and that the central patterns of the coefficient estimates remain similar to those in our main estimates in the final column of Table 3, with the exception that the previously marginally significant HAZ score is now insignificant (p = 0.16).
The parameter estimates in the final model are shown and also details of which of the variables are centred.
The final parameter estimates in the final analysis are shown in Table 3.
Removing these patients from the analysis produced negligible changes in the estimates in the final model.
We examined a wide variety of variables; thus, estimates in the final model with a 95% CI close to including the null value should be interpreted with caution.
Our results are presented without adjustment for these covariates because of their lack impact on the estimates in the final models.
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Factor intercorrelations were estimated in the final multilevel factor model using M plus.
Allele (nested) effects for each QTL within family were estimated in the final optimized QTL model.
Regions of 90% credibility were computed from the distribution of F values estimated in the final run.
The separate residual variances (RUV) for the different assays were not significant; hence, only one RUV parameter was estimated in the final model.
Odds ratios and their associated 95% CI were estimated in the final model for factors statistically significantly associated with the presence of E. coli O157.
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