VariantPlex® DNA Tests


Archer® VariantPlex panels combine patented enrichment chemistry, an easy workflow and powerful bioinformatics to generate target-enriched libraries from deoxyribonucleic acid (DNA) to confidently detect copy number variations (CNVs), single-nucleotide variants (SNVs) and indels by next-generation sequencing (NGS).
Key Features
Low input

Anchored Multiplex PCR (AMP™) chemistry was purpose-built for library prep from low-input and degraded samples such as FFPE tissue.

Sensitive & specific variant detection

Error correction features within Archer Analysis remove sequencer noise to reveal mutations below standard next-generation sequencing NGS-based detection thresholds.

Quantitative CNV detection

Molecular barcode-driven unique molecule counting provides robust copy number analysis.

Exceptional coverage

AMP chemistry provides complete, strand-specific and bidirectional coverage of target exons to maximize variant detection.

Complex mutation detection

Exceptional coverage combined with powerful bioinformatics enable mutation detection in traditionally difficult regions like CEBPA & FLT3.

Customization

Create from scratch or modify any panel below to keep up with the pace of discovery.

Get Started Now
Catalog panels that are on the shelf and ready for delivery
  • 1 Gene
  • 500K Reads
  • 37 Genes
  • 3M Reads
  • 75 Genes
  • 4M Reads
  • 67 Genes
  • 2.5M Reads
Predesigned panels that can be delivered in 3-4 weeks
  • 11 Genes
  • 750K Reads
  • 2 or 3 Genes
  • 500K Reads
  • 1 Gene
  • 100K Reads
  • 20 Genes
  • 750K Reads

Build your own panel or modify an assay

  • 100s to Choose From

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