Clinical Genomics, also known as clinicogenomics, is the study of clinical outcomes with genomic information. Genomic factors have casual impact on clinical knowledge. Clinicogenomics uses the complete genome of a patient so as to diagnose diseases or modify medications solely for the patient. Whole genome testing can discover a lot of additional mutations and structural anomalies than targeted gene testing. Moreover, targeted gene testing can solely test for the diseases that the doctor screens, whereas testing the entire genome screens for all diseases with best known markers directly.
- Track 1-1 Polymerase Chain Reaction
- Track 2-2 Karyotyping
- Track 3-3 Quantitative fluorescent PCR
- Track 4-4 Multiplex Ligation Probe Amplification (MLPA)