Tailored Pharmacogenomics Solution
Custom assay development
We offer customized, end-to-end pharmacogenetics (PGx) solutions by leveraging our decades of experience in genomics translational research and clinical testing. We specialize in in-depth data analysis and clinical interpretation to help our partners develop better therapies for tomorrow. Whether you are looking for a single gene test, a high-throughput scan of all known PGx markers, or a custom assay, we are uniquely positioned to develop the tailored, end-to-end solution for you.
Read more about our expertise in CYP2D6 analysis.
Data analysis and end-to-end interpretation
High quality bioinformatics analysis and in-depth interpretation to translate the complex genetics data into clinical insights is the key to the success of a PGx project. RPRD’s team of expert has a long history of pioneering translational genomics research, contributing to the knowledge base of PGx, and establishing its clinical utility. Leveraging our nearly 20 years of experience, our PGx experts provide unique genetic insights to guide clinical trial design and improve drug discovery process.
commonly ordered PGx genes
| Phase I Enzymes | Phase II Enzymes | Transporters | Modifiers |
|---|---|---|---|
| P450 enzyme (e.g. CYP2D6, CYP2C9, CYP2C19, CYP3A4) | UGT (e.g. UGT1A1, UGT1A8), GST (e.g. GSTM1, GSTM3), NAT (e.g. NAT1, NAT2) SULT (e.g. SULT1A1, SULT1A4), etc. | ABC transporter (e.g. ABCB1, ABCG2) SLC (e.g. SLCO5A1, SLC6A4), etc. | KCNQ1, CFTR, HBB, etc. |
Expert in a full portfolio of genomic technologies
We provide free consultation to help formulate the best testing strategy to meet the goals of your project, using a full range of state-of-the-art genomic technologies.
Next Generation Sequencing
- Detects both known and novel variants
- Highly scalable to large sample volume
- Cost effective with sample batching
- Rapid turnaround time
Real-time PCR
- Customizable number of SNPs
- Detects copy number variations (CNVs)
- Cost effective with low sample volume
- Rapid turnaround time
Microarray
- Broad coverage of SNPs
- Highly scalable to large sample volume
- Cost effective with sample batching
custom analysis and interpretation
RPRD’s experience in precision medicine offers custom analysis and interpretation to translate complex genomics information into clinical insights.
PharmacoScan Solution
Comprehensive analysis of known PGx markers in a single assay for clinical trials