The morphology, modulus and adhesion mapping were measured under different temperatures in Fig. 2.
Slice selective T1 mapping was measured with a single slice partial saturation inversion recovery RARE sequence (TI of 0.02 s, 0.5 s, 1.0 s, 1.5 s, 2.0 s, 3.0 s, 5.0 s, 10.0 s).
The linearity of the mapping was measured by the correlation coefficient (Pearson r) between the ranks of the ratings and the positions (PR), for each Participant across Categories of ratings (n = 5), and for the whole group across the set of Participant x Category (n = 100).
Thus, the recall of stochastic mapping was measured with a cutoff that corresponds to an FPR, which is equal to (or slightly lower than) that of the maximum parsimony approach.
Moreover these results assume that the DN map is measured only on an open subset of the boundary.
1.5 we consider the partial data problem, that is the case when the DN map is measured on a part of the boundary.
The latter paper contains a global identifiability result where it is assumed that the DN map is measured on any open subset of the boundary of a strictly convex domain for all functions supported, roughly, on the complement.
Isakov [95] proved a uniqueness result in dimension three or higher when the DN map is given on an arbitrary part of the boundary assuming that the remaining part is an open subset of a plane or a sphere and the DN map is measured on the plane or sphere.
Systolic (SBP), diastolic (DBP), and mean arterial blood pressure (MAP) were measured repeatedly before and after blood flow measurements on the upper arm by an automated oscillometric device (HP-CMS patient monitor; Hewlett Packard, Palo Alto, CA).
PPV, CI and MAP were measured using the non-invasive finger arterial blood pressure measurement device ccNexfin (Edwards Lifesciences BMEYE, Amsterdam, the Netherlands).
