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The differences in responses between subtypes were estimated by the χ2 test or Fisher's exact test.
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The evolutionary rates in different subtypes were estimated by considering the relaxed clock rates corresponding to branches of particular subtypes.
Associations between the length of residence and subtypes of PTD were estimated as relative risks (RRs) with 95% confidence intervals (CIs) from multivariable models.
Small differences in aberrant cell estimates between subtypes were observed (P = 0.003, ANOVA), with the luminal subtypes, generally associated with ER-positivity, showing the highest estimates (P = 0.00004, Wilcoxon's test, luminal subtypes versus remaining subgroups combined).
All three assays identified the ERV subtype accurately and no cross-reactivity between subtypes were observed.
Though researchers aren't sure how many people have this subtype, it's estimated to affect between 15percentand30percentcent of sinusitis patients.
Subtype A/+CRF02_AG was estimated to be the second leading cause of the pandemic (27%), followed by subtype B strains (12.3%).
For each of the two classification schemes (risk category or subtype), the pair-wise concordance between sites was estimated as the fraction of all possible comparisons that were concordant and an exact-type 95% confidence interval was calculated.
However, significant variation in rates between subtypes was observed.
Differential expression of genes between subtypes was determined using DESeq2.
The relative affinities of the subtypes for chromatin can be estimated from the equilibrium distribution of the subtypes between chromatin and SAR, provided the relative affinities of the subtypes for the SAR are known.
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