FIGURE 1.

A prospective view of the use of pharmacogenomics in modern medicine. Every person (sick or healthy individuals) will undergo comprehensive genomic screening before going to the physician/clinicians. The genetic variations in all pharmacogenes of an individual will be identified through data annotation and visualization by specific bioinformatics tools. The final report for each individual will be available through a private portable PGx electronic card. PGx trained clinicians will use an individual’s genetic make-up report to tailor treatment to the patient’s needs.