It is the salient new feature of MHS that two interferograms are acquired with different directionality of time evolution, that is, one is sampled forward from time t = 0 to the maximal evolution time tmax, while the second is sampled backward from t = 0 to −tmax.
In these cases, for a single x, y-position, multiple images (2 or 3) were acquired with different z-positions.
In general, comparable or higher SL production compared to the control group was acquired with different pH regulator.
However, there are cases, especially in medicine, where the two datasets, i.e., reference and moving, are acquired with different configurations leading to contrast enhancement (i.e., pre- and post-contrast agent with magnetic resonance imaging).
Camera response data are acquired with different measurement accuracies: we gradually reduce the measurement quality of the imaging system by changing the current of the LEDs of the light source from 100%to70%0% in steps of 10% (related to the current feed of a well-calibrated case, called scenario 1 below), thus simulating a potential technical defect of the system.
Ten data sets were acquired with different orientations of the sample arm fiber to determine the average PMD depth shift of the system.
Projection images can be acquired with three different "fields of view" (FOVs): small (S), medium (M), and large (L).
Images were acquired with three different MR protocols yielding contrast dependent on spin lattice relaxation (T1), spin spin relaxation (T2), and magnetic susceptibility (T2*).
The second dataset, which we call here the lab set, was acquired with a different apparatus, a machine-to-machine, or M2M, GSM/GPRS module [21], which can be driven using standard and manufacturer-specific AT modem commands.
For three-dimensional bioluminescence imaging in the pancreatic cancer model, bioluminescence images were acquired with three different wavelength (600±10, 620±10, 640±10 nm) of bioluminescence filters.
