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Regional body fat distribution was characterised as central fat mass (CFM) and appendicular fat mass (AFM), as previously described [ 25].
The GP's distribution was characterised by three distinct peaks at 0, 2 and 9 mismatches respectively (Fig. S2).
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The perilymphatic distribution is characterised by presence of nodules along the peribronchovascular interstitium, interlobular septa and subpleural areas.
The von Mises distribution is characterised by a mean (tilde {theta }) and a concentration κ, and is given by fleft(hat{theta}_{tk}, {Huge|}, mathcal{H}_{s}; tilde{theta}, kapparight) = c_{mathcal{M}} kappa), mathrm{e}^{kappa, {text{cos}}left(hat{theta}_{tk}-tilde{theta}right)}.
Isolation, genetic drift and perhaps selection have contributed to a genetic differentiation, and the HLA loci distribution is characterised by a very high number of rare haplotypes and by a small number of very frequent haplotypes [37].
The normal distribution is characterised by very smooth slopes on both flanks of the distribution.
Furthermore, effects on haemodynamics, oxygenation and ventilation/perfusion (V ⋅ / Q ⋅ ) distribution are characterised.
First, every coverage distribution is characterised by extreme overdispersion as the variance is greater than the mean in each sample (Table 1 and Figure 1B).
Representative OMA with well differentiated pore size distributions were characterised by N2 adsorption, XRD and TEM.
Glucose and insulin concentration distributions were characterised and compared by sex and BMI category.
Both TE distributions are characterised by two kinds of sites: sites with low and sites with high (>10%) insertion frequencies.
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