The translocase activity of MtbMfd was measured on linear triplex DNA substrate by carrying out TFO (Triplex Forming Oligonucleotide) displacement assay described previously for EcoMfd [23].
For the antigen expression which was normalized to cell size, the fluorescence of the conjugated monoclonal antibodies as well as the forward scatter signals were measured on linear scale.
The relevance measures based on linear correlation and symmetrical uncertainty select those time instants in the systole and diastole, where normal heart murmurs should be present.
Finally, the time course of treatment of each individual will be modeled by projecting the outcome measures on orthogonal linear, and quadratic of time.
Cstat, static compliance computed as tidal volume/(Pplat at low PEEP-low PEEP); Clin, linear compliance measured on the linear part of the pressure-volume curve; values of p for the comparison were calculated for low PEEP versus high PEEP; values are expressed as median (interquartile range).
Gating was set on side-scatter, then by the fluorescence measured on a linear scale.
The forward scatter and side scatter were measured on a linear scale, whereas green fluorescence was registered on a log scale.
The PI fluorescence was measured on a linear scale using a FACS Cyan flow cytometer (Dako, Glostrup, Denmark), while the Ki67 staining was analysed using a BD FACSCanto II flow cytometer.
Radial FWHM was measured on four linear sources and ranged from 2.35 mm to 2.48 mm for PSF reconstruction and from 6.19 mm to 6.46 mm for OSEM reconstruction.
The measure is based on linear vector autoregressive (VAR) modelling: suppose that the (again, possibly multivariate) "predictee" process X t is modelled as a vector linear regression on its own past, as well as on the past of the "predictor" process Y t : X t = A 1 X t − 1 + A 2 X t − 2 + … + B 1 Y t − 1 + B 2 Y t − 2 + … + ε t (8).
