Inherited Disease Tests

Archer® VariantPlex® panels for inherited diseases are highly customizable tests that deliver comprehensive coverage of target exons for genes associated with breast cancer risk (BRCA 1/2 & PALB2) and cystic fibrosis (CFTR).
Key Features
Safeguard against allelic dropout

Dual, independent coverage across target regions ensures that coverage is retained when one primer drops out due to primer-blocking SNVs.

Exceptional coverage

Anchored Multiplex PCR (AMP™) chemistry provides complete, strand-specific and bidirectional coverage of target exons to maximize variant detection.

Single-day lyophilized workflow

Easy-to-handle lyophilized reagents and a simple workflow mean libraries can be made in a single day.

Customization

Create from scratch or modify either panel below to match the pace of discovery.

Get Started Now

Catalog panels that are on the shelf and ready for delivery
  • 1 Gene
  • 150K Reads
Predesigned panels that can be delivered in 3-4 weeks
  • 2 or 3 Genes
  • 500k Reads

Build your own panel or modify an assay

  • 100s to Choose From

This website stores cookies on your computer. These cookies are used to improve your website and provide more personalized services to you, both on this website and through other media. To find out more about the cookies we use, see our Privacy Policy.

We won’t track your information when you visit our site. But in order to comply with your preferences, we’ll have to use just one tiny cookie so that you’re not asked to make this choice again.