Tailored Pharmacogenomics Solution

DNA strand for Precision Medicine

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.

Examples of highly actionable PGx genes

CACNA1S

CFTR

CYP2B6

CYP2C9

CYP2C19

CYP2D6

CYP3A5

CYP4F2

DPYD

G6PD

HLA-A and HLA-B

IFNL3

NUDT15

RYR1

SLCO1B1

TPMT

UGT1A1

VKORC1

Interested in the other markers?

commonly ordered PGx genes
Phase I EnzymesPhase II EnzymesTransportersModifiers
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
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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