What if you could…
- Perform single-nucleotide polymorphism, copy number variation and tandem repeat assays in a single qPCR workflow
- Get results in half the time
- Get 100% coverage of AMP Tier 1 CYP2D6 targets, including difficult-to-detect star alleles such as *29
Why choose the Advanta™ Pharmacogenomics Assay?
One workflow for everything
Perform SNP, CNV and tandem repeat analysis in a single integrated qPCR workflow.
Biomark™ systems provide one workflow on one system
Example: Seamlessly detect key variants like UGT1A1 (rs3064744) and others.
Advanta PGx Core Panel
Core panel coverage
- Targets variants in 17 genes implicated in drug metabolism pathways
- Covers 71 SNPs/indels, three CNV markers and RNase P (control)
Create a panel that meets your research needs, whether focused on drug response or rare variant detection.
Why choose our PGx solutions?
All-in-one flexibility
Whether using a predefined panel or designing a custom solution, our platform handles it all in a single workflow.
Future-proof your lab
Easily adapt to new guidelines, regulations and research needs by adding or modifying assays as required, leveraging the flexibility of our platform.
Comprehensive insights
With the most accurate and comprehensive detection of critical variants like CYP2D6, UGT1A1 and NUDT15, no other platform offers such precise pharmacogenomic insights in a single run.
