
PGXperts Interpretation as a Service
PGx interpretation – modular, scalable, and reliable
PGXperts Interpretation as a Service (IaaS) converts complex genetic data into evidence-based and actionable pharmacogenetic (PGx) insights.
Benefit from a user-friendly solution that saves time, delivers precise results and is tailored to your requirements.
References
Three steps
Interoperability
Why PGXperts
IaaS was developed for both clinical and research environments
and bridges the gap between scientific knowledge and practical application.
Researchers receive fully automated support in precisely interpreting gene variants and making them scientifically usable.
Medical professionals receive reliable information for prescribing personalized medication for their patients.
IaaS is in use across Europe


Create your customized report
in just three steps
Define report type & genes
Set technology
Configure report

1. Define report type & genes
Which genes would you like to examine?
Select the desired area of application and define your panel. Select genes, drugs, and gene-drug pairs that are relevant to your use case.
2. Select technology
We are technology-agnostic
There are several genotyping technologies suitable for pharmacogenetic testing, each offering its own benefits. PGXperts is compatible with established PCR systems, microarrays, and hybrid platforms. Choose from industry-leading technologies to suit your needs.


3. Configure report
Modular, clear, practical
We provide you with a versatile reporting solution that combines genotyping data and pharmacogenetic interpretations in a clearly structured, user-friendly format.
Modularly structure your content, customize language, select terminology and design the branding of your reports.
Evidence-based data on
Genes
Active substances
Genetic variants
The PGXperts database is built on international guidelines (e.g., CPIC, DPWG, SEFF) and recommendations from regulatory authorities (e.g., EMA, FDA, Swissmedic). Relevant genetic variants are identified according to official definitions (e.g., CPIC or PharmVar) and selected following the recommendations of the Association for Molecular Pathology (AMP).
Interoperability
When every interface becomes a door opener
PGXperts IaaS integrates seamlessly with existing bioinformatics pipelines, laboratory information systems (LIMS) and secondary analysis tools. Structured content and formats ensure that information can be incorporated directly into clinical systems.
Learn more about how PGXperts PRiM makes this data usable in routine clinical practice.
Integration via REST-API
Standardized nomenclature
Structured data export (JSON format)
Phenotype profile as a data matrix
Pharmacogenetics is the key to Personalized Medication
Pharmacogenetics studies how our genes influence the effectiveness and safety of medications. It enables safe and effective drug therapy tailored to the individual genetics of each patient.
Why PGXperts
Why should you
choose PGXperts?
Installation
We are your reliable PGx partner
We believe in true collaboration and are committed to building long-term partnerships, tailoring every solution to your operational goals and workflow requirements. Our team supports you from needs analysis and setup to validation, staff training and beyond.

Gregor Malischnig
Head of Sales & Business Development – PGx
Contact
Expand your service with PGx interpretation from PGXperts!
We will be delighted to introduce you to the features and benefits of PGXperts IaaS. Schedule a meeting with your personal consultant today!
Downloads
More information
Select genes
ABCG2
CYP3A4
HLA-A
SLC47A1
VKORC1
CYP2B6
CYP3A5
HLA-B
SLCO1B1
CYP2C9+VKORC1
CYP2C19
DPYD
IFNL3
SLC22A2
NUDT15+TPMT
CYP2C9
G6PD
NUDT15
TPMT
… … More on request
CYP2D6
GSTP1
SLC22A1
UGT1A1
Thermo Fisher
| Technology | Content | Supported instruments | Supported products |
| Real-time PCR (qPCR) | SNP Genotyping, Copy Number Variation | QuantStudio™ 12K Flex and equivalent systems with 384 well-blocks (QuantStudio 5, QuantStudio 7) |
TaqMan™ SNP Genotyping Assays, TaqMan™ copy number assays,
|
| Digital PCR (dPCR) | Allele–specific Copy Number Variation, Copy Number Variation with high resolution | QuantStudio™ 3D, QuantStudio™ Absolute Q™ Digital PCR System | TaqMan™ SNP Genotyping Assays, TaqMan™ copy number assays |
| Microarrays | SNP Genotyping, Copy Number Variation | GeneTitan™ Multi-Channel Instrument | Axiom™ PharmacoScan™, Axiom™ PangenomiX Plus |
Illumina
| Technology | Content | Supported instruments | Supported products |
| Microarrays | SNP Genotyping, | iScan™ System |
Infinium Global Diversity Array (GDA) with Enhanced PGx, Infinium™ Global Screening Array (GSA) with Enhanced PGx
|
Select type of interpretation
| Module | Laboratory results of genotyping | Phenotype profile | PGx profile | PGx profile and medical implications | PerforM |
| General information | |||||
| Metabolism types Metabolism of medication | |||||
| Medications Risks and potential side effects | |||||
| Impact Clinical consequences and measures | |||||
| Immediate effects Measures regarding current medication |
Output formats
For broad use of the data obtained, we offer export options for the report as GUI, JSON, and PDF files.

