Pharmacogenomics for drug personalisation
A pharmacogenomics test (PGx) that shows how your genes affect drug metabolism. CoGenesis® Drug Response uses PGx to identify how your genes affect your response to common drugs. This helps doctors choose the right drug and dose for you.
| Step / Test | Accuracy | Notes |
|---|---|---|
| Variant calling – SNP | >99.9% | |
| Variant calling – Indel | >99% |
4mL peripheral blood (EDTA), 2mL saliva, 4 buccal swabs
Preferred sample type:
Saliva or buccal swab sample collection: Follow the enclosed instructions; do not eat, drink, or smoke for 30 minutes before collection.
Samples must be collected and submitted by a licensed healthcare professional.
Please contact us for institutional pricing and ordering details.
Results guide clinicians in tailoring prescriptions for safety and effectiveness, with support from relevant CPIC, DPWG or FDA guidelines.
Pharmacogenomics (PGx) is the study of how genetic differences influence an individual’s response to medications. Variations in genes that encode drug‑metabolizing enzymes, transporters, and drug targets can significantly affect drug absorption, distribution, metabolism, and elimination. For example, polymorphisms in CYP450 enzymes (such as CYP2D6, CYP2C19, and CYP3A4) can lead to rapid, normal, or poor metabolism of many commonly prescribed drugs, including antidepressants, anticoagulants, and pain medications. CoGenesis® Drug Response provides clinically actionable insights by identifying patients at risk of adverse drug reactions. Guidelines from organizations such as CPIC (Clinical Pharmacogenetics Implementation Consortium), DPWG (Dutch Pharmacogenetics Working Group), and the FDA support the integration of PGx into clinical practice. By tailoring drug choice and dosage to a patient’s genetic profile, PGx may enable safer, more effective, and personalized treatment strategies, reducing trial‑and‑error prescribing and improving overall outcomes.