Multitest analysis of an individual's blood provides a biochemical profile that reflects his identity and pathophysiological state. During a six-week period we repeatedly profiled 10 volunteers for 22 different analytes, using continuous-flow and discrete analyzers (SMAC, KA 150 enzyme analyzer, ABA-100, AutoAnalyzers) and manual procedures. Two years later, we obtained multiple follow-up profiles. Using linear discriminant functions derived from the first five (or first 10) specimens from each subject, we were able correctly to identify 96% (or 100%) of the specimens collected during the remainder of the six-week testing period. Ninety percent of the two-year follow-up specimens were correctly identified when we used all the original profiles to calculate the discriminant functions. Deliberately mislabeled specimens were also correctly identified by discriminant analysis. Profiles of individual samples (and average profiles for each subject) were graphically displayed as computer-drawn faces and non-linear maps. Covariances between pairs of tests on repeated profiles differed significantly for different subjects. Inter-test relationships were graphically displayed by nonlinear mapping.