From genetic data to clear clinical guidance

Pharmacogenetic interpretation

Actionable report

Results are delivered as an easy-to-read report, ready for integration into healthcare IT systems.

Rapid turnaround

Our interpretation service processes data quickly, delivering results in 1-3 business days.

Scalable solution

Designed to meet the needs of laboratories, hospitals, pharmaceutical companies, and research environments.

Turn genetic insights into safer prescribing

Abomics’ interpretation service makes personalized medicine simple. Laboratories upload patient’s genetic data, and we transform it into a clear, clinically relevant report. This patient specific report provides a genetic profile and recommendations to support safer and effective prescribing. Delivered securely and designed for seamless integration into clinical workflows, this service ensures that precision medicine becomes part of everyday care.

Ready to bring personalized treatment into practice?

How the PGx interpretation process works

Doctor’s consultation

The clinician initiates a pharmacogenetic test through the standard laboratory order process.

Collection of patient sample

Blood sample or a cheek swab is collected in a laboratory.

Laboratory analysis

Sample is analyzed in a laboratory that generates a genetic data.

Pharmacogenetic interpretation

Data is processed in our interpretation workflow to produce a comprehensive PGx report.

Delivery of results

The PGx report is delivered to the clinician and optionally to the patient.

Personalized pharmacogenetic report

Abomics’ pharmacogenetic report is a clear, actionable guide designed to help healthcare professionals make safer, smarter prescribing decisions.

What's included in the PGx report?

Patient-specific genetic profile

Genotypes and phenotypes relevant to drug metabolism.

Medication guidance

Drug-specific alerts and recommended dose adjustments based on genetic variants.

Clinical interpretation

Clear, actionable recommendations aligned with international guidelines

Specialty-based information

Pharmacogenetic recommendations and clinical insights grouped by medical specialty.

Easy-to-read summary

Summary contains tested genes and their predicted phenotypes.

Patient access

QR-code for Abomics’ portal and PIN code access (optional).

Key features of PGx interpretation service

Genetic information
Genotypes & phenotypes
Medication information
Drug alerts & dosing guidance
Approved interpretation
Reviewed by Abomics’ pharmacogenetic experts
Fast delivery
Turnaround time 1-3 business days
Secure format
PDF or EMR-ready structured data
API integration
Enables interoperability with health care IT solutions
Multilingual
Currently available in 8 languages
Security and compliance
ISO 13485 certified & GDPR-compliant
Patient Portal
Optional access to Abomics patient portal GeneAccount
Regular updates
Aligned with scientific guidelines for reliable results

Why healthcare professionals choose Abomics?

Partner with a pioneer in pharmacogenetics to deliver secure, easy-to-use, and clinically validated solutions for personalized treatment decisions.
Here is why healthcare professionals trust us:
Deep expertise in pharmacogenetics
Seamless integration with health IT systems
Certified quality and compliance
Global reach with a multilingual platform
Tailored solutions to meet your needs
Questions about our PGx solutions? We are here to help.
© Abomics Oy. All rights reserved.

Sami Miettinen

Lorem ipsum dolor sit amet, consectetur adipiscing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.
  • sami.miettinen@abomicspgx.com
  • linkedin/sami-miettinen