November 10, 2026
A connected workflow for pharmacogenomics research
Paragon Genomics and Intelliseq have announced a partnership connecting the CleanPlex® Pharmacogenomics Kit with the iFlow Platform and GeneSpect PGx Reporter. The collaboration brings library preparation, downstream analysis and reporting into one integrated research workflow.
Paragon Genomics provides the amplicon-based NGS library preparation, while Intelliseq provides automated secondary analysis, star-allele calling, phenotype prediction and structured PGx reporting.
From target enrichment to PGx insights
- Prepare with CleanPlex®. Create amplicon-based NGS libraries using the CleanPlex Pharmacogenomics Kit.
- Sequence on a compatible NGS platform. Generate sequencing data for downstream analysis.
- Analyze with Intelliseq. Use the iFlow Platform and GeneSpect PGx Reporter for automated analysis, star-allele calling and phenotype prediction.
- Review PGx findings. Explore structured reports on gene–drug interactions to support expert review and research.
Start with the CleanPlex Pharmacogenomics Kit
The CleanPlex Pharmacogenomics Kit offers an approximately three-hour library preparation workflow, compatibility with major NGS platforms and support for high-throughput automation. Laboratories already using CleanPlex PGx panels can connect their sequencing data with Intelliseq’s analysis and reporting tools.
Explore the CleanPlex Pharmacogenomics Kit or contact the Paragon Genomics team to learn more.
Meet us at AMP 2026 in Seattle
Visit Paragon Genomics at Booth #1911 and Intelliseq at Booth #1904.
Join Yutao Fu, PhD, of Paragon Genomics and Klaudia Pacewicz of Intelliseq for a joint Innovation Spotlight on Friday, November 13, 2026, from 12:40–1:10 PM PST at Innovation Spotlight Stage #2.
Read the full press release on GlobeNewswire.
CleanPlex® PGx panels are for Research Use Only. Not for use in diagnostic procedures.