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Pharmacogenomics

Determine optimal prescriptions by analyzing drug efficacy and side effect risk based on your patient’s genetic profile.

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sequence once, query often®

TURNAROUND

New Patient

6-9 days

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SAMPLE

Saliva, Blood, Buccal

One comprehensive test provides clinical answers today and enables future queries as science evolves.


New patient
6-9 days
Existing patient
≤ 5 minutes*

Clinical Utility

Identifies individuals who may benefit from:

  • Medication selection tailored to their genetics
  • Dose adjustments to reduce risk of medication side effects or to improve medication effectiveness
  • More informed treatment decisions over time

TECH SPECS

Methodology

Whole gene sequencing using the Exome+® NGS (exome capture + deep intronic coverage in key regions).

Informatics

Special informatics applied to star alleles, including CYP2D6-CYP2D7 hybrid alleles, where up to five haplotypes can be detected.

Accuracy

> 99.9% across the full reportable range.

Helix pharmacogenomics panels comparison

View a full comparison of all Helix Pharmacogenomics tests here:

Helix Pharmacogenomics Panels