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To address this problem, local region intensity information is incorporated into the energy function [ 29– 36].
A seed-point in the cellular background was selected and propagated to the entire image stack, using a threshold of 30% of the mean region intensity as the voxel inclusion criterion.
We investigated potential sources of heterogeneity through a series of analyses, sub-grouping the trials by: geographical region, intensity of malaria transmission (low to moderate versus high malaria transmission), known parasite resistance, allocation concealment, participant age, and drug dose (comparing regimens where there are significant variations in drug dose).
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Comparisons of these and the upstream/downstream region intensities were determined to identify shear-induced changes in GFP levels.
The threshold of both DHPR and Dys fluorescence channels was determined from the background region lying outside the fibres using the statistics of those regions' intensity histograms.
In cases in which there were tumor cell populations within one sample with clear distinction in staining intensities, each region's intensity was multiplied by the appropriate percentage and added to produce the sample score.
Average region pixel intensity [ 21 ]: the CAD computes the average pixel intensity value for all the labeled "chromosomes" on the image.
Standard deviation (STD) of the region pixel intensity [ 21 ]: the CAD first computes the average pixel intensity for each labeled region and then calculates the standard deviation of the region pixel intensity for all the labeled "chromosomes".
The most intensive signal is a broad absorption in 1600 2100 nm region, the intensity and λmax is increasing with the size of the central metal.
For each time point and each skin region relative intensity values were calculated.
Obviously, in the low concentration region, SERS intensity decreased with the test concentration decreases.
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