Reliable, Precise Detection

  • Detect SNPs, indel variations, and CNVs in a single assay.
  • Haplotype reports are rapidly generated from genotyping data with automated software tools.
  • 96- and 384-well formats offer the flexibility to generate results from 10s to 1000s of samples a day.

iPLEX® PGx Pro Panel

Covers 99% of the most relevant pharmacogenetic markers considered to be broadly applicable to clinical trials. Interrogates 191 SNPs in 36 key genes, including CYP2C9, CYP2C19, CYP2D6, and UGT1A1.
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iPLEX® PGx 74 Panel

Targets the most relevant variants in 20 principal genes implicated in drug metabolism pathways. Interrogates 69 SNPs/INDELs, plus 5 CNVs.
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Obtain biologically-relevant data for most of the known haplotypes of each gene. Interrogates 38 SNPs in CYP2C9 and 11 SNPs in VKORC1.
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iPLEX CYP2C19 Panel

Investigate and confirm pharmacogenetic biomarkers in CYP2C19. The panel contains assays for 31 SNPs, covering most of the known CYP2C19 haplotypes.
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iPLEX CYP2D6 Panel

The CYP2D6 Panel is a set of 30 SNP and 5 CNV assays, covering most of the known CYP2D6 haplotypes.
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Pharmacogenetic Solutions Brochure