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The tortuous model for the pore length (L f) becomes identical to the general fractal model for length (L) if (L_{s}^{{D_{T} }}) is a constant coefficient, and tortuosity fractal dimension (D T) is set equal to the fractal dimension that controls the length (D l).
Moreover, V-Phaser 2 has a clear model for length polymorphic variants, which is particularly relevant for the study of chronic diseases like HIV.
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A model involving additive effects of spp, FnF, and FL, but not HW, had nearly the same level of support (ΔBIC = 0.4; this was also the best-supported model for length-adjusted speeds, Table S3).
Table 6 presents the results of the linear regression modeling for length of surgery and LOS.
Adjusting these models for length of hospital stay did not affect the results.
Linear models for length of gestation were adjusted for maternal race, age, employment status and infant sex.
Final models for birth weight and crown heel length included all of the variables in models for length of gestation, except that total DAPs replaced dimethyl phosphate levels.
The final models for length of gestation included continuous variables for maternal age, week prenatal care was initiated, and dimethyl phosphate in urine at 26 weeks, as well as categorical variables for parity, mother's country of birth, family income, and smoking.
For inhospital mortality, the model controlled for length of stay and COPD.
The study of residuals in the weight model (not for length) suggested that a logarithmic transformation should improve normality.
Figure 3 shows the runtime in hours for the two models for lengths m = 0,…, 4. For m = 3 and m = 4 the time it takes to perform computations on the original model has been extrapolated from running the software for this model across 150 locations and multiplying by 40.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com