Pharmacogenetics
Advancing precision medicine research through genome diversity
Every genome is unique.
Every decision begins with understanding it.
Accessibility
Making pharmacogenetic research assays affordable, fast, and easy to integrate into everyday laboratory workflows.
Comprehensiveness
Offering broad genetic coverage of pharmacogenetically informative variants is crucial to truly advance precision medicine research.
Providing bioinformatic tools to support researchers in interpreting complex genetic variants, translating genetic data into structured, meaningful research insights.
Discover our complete solutions for pharmacogenetics profiling
EasyPGX®
The Dy qPCR solution for Pharmacogenetics research
For research use only. Not for use in diagnostic procedures.
Ready to use
Fast
Easy
Comprehensive DPYD and UGT1A1 Genotyping — Simplified with EasyPGX®
EasyPGX® combines fast turnaround, intuitive workflow, and complete variant detection, supporting robust and reliable pharmacogenetic research.
DPYD
EasyPGX Ready DPYD allow the detection, by allelic discrimination, of DPYD gene mutations:
- DPYD (IVS10C>G, HapB3)
- DPYD*13 (c.1679T>G)
- DPYD*2A (IVS14+1G>A, c.1905+1G>A)
- DPYD c.2846A>T
- DPYD*6 c.2194G>A
UGT1A1
EasyPGX Ready UGT1A1 allow the detection, by allelic discrimination, of UGT1A1 gene mutations:
- UGT1A1*28
- UGT1A1*6
EasyPGX® workflow
Join the precision oncology research revolution with EasyPGX® System
Nucleic Acid extraction
PCR setup
Add extracted samples to ready-to-use 8-well strip
<5 min
TURNAROUND TIME
<5 min
HANDS-ON
PCR run
Load the strip onto the thermal-cycler and start the run
90 min
TURNAROUND TIME
<1 min
HANDS-ON
Data analysis
Import raw data into the EasyPGX® Analysis Software
<1 min
TURNAROUND TIME
<1 min
HANDS-ON
EasyPGX® Analysis Software
Streamline your data analysis process
EasyPGX® Analysis Software is the dedicated automated data analysis solution designed for use with EasyPGX® ready-to-use kits.
- No cloud or external data sharing required
- Data analysis and raw data checking in a single software solution.
- Data export and reporting available in various common file formats.
For research use only. Not for use in diagnostic procedures.
EasyPGX® products may be covered by third-party patents or other intellectual property rights; depending on the jurisdiction, purchase of the product may not include a license to use such patents.
Myriapod® NGS PGX Sign Panel
Advanced Pharmacogenetics Signature for precision medicine research
The Myriapod® NGS PGX Sign Panel is an advanced NGS-based solution for comprehensive pharmacogenetics profiling in research, analyzing genomic variants across key ADME-related genes.
For research use only. Not for use in diagnostic procedures.
Ready-To-Use
Easy& Fast
Comprehensive
A comprehensive tool
for pharmacogenomic research.
20 genes- extensive gene coverage
> 1000 SNV analysed
Integrated data management system
Myriapod® NGS workflow
NGS made Easy.
Results made Faster
Library prep
Indexing
Pooling and
quantification
Sequencing
Data
analysis
<3 days
TURNAROUND TIME
Myriapod® NGS Data Analysis
On-Premise Bioinformatics for genomic research.
The Myriapod® NGS Data Analysis suite is a robust, on-premise bioinformatics solution combining a high-performance workstation with proprietary software for streamlined NGS data processing, even in a non-bioinformatic expert environment.
- Smart Variant Analysis: SNVs, InDels, CNV automatically identified – no bioinformatics expertise needed.
- Total Data Protection: 100% local processing. No cloud. No external servers. No compromises.
- QC You Can Trust: Automatic run and sample validation, every time.
- Built-In Intelligence: Variants are classified instantly using trusted genomic databases.
For research use only. Not for use in diagnostic procedures.