Archer DX

Disease State

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).

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Liquid Biopsy Tests


The Archer® LiquidPlex panel for Illumina® is an advanced and user-friendly solution for targeted next-generation sequencing (NGS) of circulating cell-free tumor DNA (ccfDNA/cfDNA/ctDNA) from 28 genes commonly associated with solid tumor type cancers.

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Immune Repertoire Analysis


Archer® Immunoverse™ panels are targeted next-generation sequencing (NGS) tests to characterize the human immune repertoire from RNA input. Powered by Anchored Multiplex PCR (AMP™), the lyophilized reagents uniquely tag and amplify V(D)J rearrangements for clonotype identification and frequency reporting.

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NTRK Fusion Detection

NTRK fusions are critical events in cancer genomics and are notoriously difficult to detect. Archer® FusionPlex® next-generation sequencing (NGS) tests provide sensitive NTRK fusion detection without prior knowledge of fusion partners.

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Blood Cancer

Archer® Blood Cancer tests detect various driver mutations in hematologic malignancies, such as myeloid and lymphoid diseases, by targeted next-generation sequencing (NGS). This approach combines FusionPlex® and VariantPlex® panels to characterize gene fusions, copy number variations (CNVs) and other variants from a single sample.

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Solid Tumor

Archer® Solid Tumor tests provide a targeted sequencing approach to detect various driver mutation types in solid tumors. This approach combines FusionPlex®, VariantPlex® and LiquidPlex™ panels to characterize gene fusions, CNVs and other variants from a single, low-input FFPE sample and liquid biopsy.

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