Power estimates for cases r > N/2 are not shown.
Proper adjustment needs to be made to obtain KM estimates for case-cohort data where cases were oversampled.
Our meta-analysis showed that while the magnitude of the ORs were inconsistent across studies, the pooled estimates for case-control studies were statistically significant for both cardiovascular disease (OR 2.20; 95% CI 1.49 - 3.26) and hypertension (OR 1.48, 95% CI 1.22 - 1.78).
Risk estimates for cases with head and neck SCC were similar to those with SCC tumours at other anatomic sites (data not shown).
Primary analyses considered the exposure by quintiles of the exposure metric, defined among the exposure estimates for cases at their diagnosis age.
The ERR/Gy estimates for cases with direct interviews < 2 years from start of chemotherapy (ERR/Gy = –0.47) and the remaining cases (ERR/Gy = 2.38) differed significantly (p = 0.021), with the former estimate incompatible with our current understanding of radiation-related leukemia risk.
With this constraint, four unknown parameters were estimated for Case 1, while five unknown parameters were estimated for Case 2, using the two kinetic and thermodynamic constraints of Eq. (S7), as in our previous paper on the uniporter [11] (see Materials S1).
Not only does this percentage affect the estimated number of foodborne cases of that disease, but it dominates the overall estimated percentage of gastroenteritis cases attributed to food, and thus the estimate for cases of unknown etiology.
More than 100% of the clustering effect was estimated for cases in the same counties.
We calculated a separate capture-recapture estimate for cases in each SES category within each diagnostic group.
Therefore, haplotype phase should be estimated for cases and controls separately to ensure that haplotypes in the controls do not hide the typical haplotypes in the cases.
