Research Products

Molecular profiling products

We deliver cutting-edge molecular products to laboratories and clinical researchers seeking better genomic answers. Our patented technology — Anchored Multiplex PCR (AMP™) — is at the core of our industry-leading products. We offer a suite of products and services that are accurate, personal and easy-to-use in local settings.​

Our research products include:

Blood Cancer Research Panels

Blood cancer research panels leverage a powerful technology for error-corrected next-generation sequencing for high sensitivity oncogene profiling.

Deep molecular profiling of blood cancers

Blood cancer research panels 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, point mutations, copy number variations (CNVs) and other variant types from a single sample. 

Key Features
Unified Workflow
Complex Variant Detection
Comprehensive Tumor Profiling
Confident Variant Calling

Custom Panels

Our flexible technology and design expertise enable high performance customization of biomarker targets and bespoke applications.

The NGS panel you really want

Design your own panel with genes of interest for targeted next-generation sequencing (NGS) using RNA, DNA or ctDNA. We offer three options for custom panel creation: Assay Marketplace, Assay Designer and Designer Pro.

Key Features
Expert Primer Design
Simple and Intuitive
Exceptional Performance
Full Support

Solid Tumor Research Panels

Solid tumor research panels provide a robust targeted sequencing approach to detect critical biomarkers from both liquid and tissue biopsies.

Robust molecular profiling from tissue and liquid biopsies

Solid tumor research panels offer a sensitive targeted sequencing approach for biomarker detection from both liquid and tissue biopsies. This approach leverages DNA, RNA or ctDNA input types for sensitive characterization of all variant types from low-input clinical samples. 

Key Features
Unified Workflow
Confident Variant Detection
Comprehensive Tumor Profiling
Partner Agnostic Fusion Detection
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