The proposed methodology was measured against the benchmark of statistical regression to determine its effectiveness.
The reliability of the methodology is measured through the cross validation procedure and it is observed that the procedure is valid with less than 5% error.
The watermarking performance of the proposed methodology is measured using the PSNR quality index and the Bit Error Rate (BER) [7] at the detectors' side, under various attacking conditions.
Apart from detecting peptides from proteins several times in different colonies (Dataset S3), confidence in our identification methodology was measured by controlling the false discovery rate (estimated to be about 0.25%) utilizing a decoy strategy.
Serum NGAL (ELISA methodology) was measured in 109 critically ill patients with AKI at inception of RRT in 7 ICUs of a tertiary care university hospital.
The quality of methodology are measured in three ways, cost (shown as running time), sensitivity (shown as call rate) and accuracy.
Insulin concentrations were determined by human specific radioimmunoassay (Linco St. Charles, Missouri) methodology and glucose concentrations were measured by a Stat Glucose/Lactate Analyzer Model 2000 (YSI, Yellow Springs, OH, USA).
Cell proliferation and cytokine production were measured with methodologies as described in T-cell proliferation section.
Total renin concentration, prorenin concentration, plasma angiotensinogen, PRA, and biomarkers of inflammation and endothelial dysfunction were measured using methodology described previously (4).
Using well-established methodologies, endothelial permeability was measured by the passage of FITC-conjugated 40 kDa dextran through a monolayer of human umbilical vein endothelial cells (HUVEC -expressing vGPCR [ 5, 13].
