Standalone RNA Analysis

Add RNA Insights Without Replacing Your DNA Workflow

For laboratories with an established DNA testing solution, the RNA Fusion NGS Panel provides a complementary, standalone workflow for detecting fusion events and other transcript-level alterations.

Partner-Agnostic Fusion Detection

The panel supports detection of known and novel fusion events without requiring both fusion partners or the precise breakpoint to be predefined.

Panel Coverage

Targeted RNA Fusion Coverage Across 143 Genes

Review the panel’s complete gene content and tier classification to determine how it fits your laboratory’s RNA testing workflow.

143

Fusion Genes

Total genes included in the targeted RNA Fusion NGS Panel.

58

Tier 1 & 2

Genes included within the panel’s Tier 1 and Tier 2 content.

85

Tier 3 & 4

Genes included within the panel’s Tier 3 and Tier 4 content.

Designed for Established Laboratories

A Flexible Addition to Your Oncology Testing Workflow

Extend your laboratory’s testing capabilities while preserving the DNA workflow you already have in place.

01

Standalone RNA Panel

Add RNA fusion analysis while maintaining your laboratory’s existing DNA testing workflow.

02

Known and Novel Fusions

Detect established fusion events while supporting identification of rare or previously uncharacterized fusion partners.

03

Partner-Agnostic Detection

Identify fusion events without requiring both partners or exact breakpoint locations to be programmed into the assay beforehand.

04

Broader RNA Analysis

Expand beyond fusion detection with support for additional transcript-level alterations.

RNA Variant Detection

More Than Fusion Analysis

Analyze multiple types of RNA alterations relevant to oncology research and molecular profiling.

Known and Novel Fusions

Detection of established, rare, and novel fusion events.

Splice Variants

Identification of alternative transcript-splicing events.

Exon-Skipping Events

Detection of transcript alterations involving omitted exons.

RNA SNVs and Indels

Analysis of single-nucleotide variants and small insertions or deletions detected at the RNA level.

Gene-Expression Changes

Assessment of gene-expression changes within the panel’s targeted content.

Detection depends on the genes and regions covered by the panel, specimen quality, RNA quality, and overall assay performance.
Expanded Fusion Detection

Detect Fusions Without Predefining Both Partners

Conventional targeted fusion assays may be designed to detect only specific gene pairings or previously established breakpoint locations.

The RNA Fusion NGS Panel uses a partner-agnostic approach that does not require both fusion partners or the exact breakpoint to be predefined.

This supports broader detection of known, rare, and novel fusion events while reducing dependence on a fixed list of expected fusion combinations.

  • No requirement to predefine both fusion partners
  • No requirement to assume an exact breakpoint location
  • Supports known, rare, and novel fusion detection
  • Provides additional transcript-level analysis
Complementary Testing

Designed to Work Alongside DNA Analysis

DNA and RNA analysis provide different views of tumor biology. The standalone RNA Fusion NGS Panel allows laboratories to add transcript-level analysis without replacing an existing DNA mutation panel.

  • Preserve your established DNA testing process
  • Add RNA fusion and transcript-variant analysis
  • Expand your laboratory’s oncology testing capabilities
  • Consolidate RNA analysis within a targeted NGS workflow
  • Support broader molecular profiling of tumor specimens
Laboratory-Focused Solution

Who Is This Panel For?

Molecular Laboratories

Laboratories with an established DNA NGS workflow seeking to add complementary RNA analysis.

Oncology Laboratories

Laboratories expanding their oncology testing capabilities to include fusion and transcript-level analysis.

Reference Laboratories

Laboratories developing broader tumor-profiling menus across multiple oncology applications.

Research Laboratories

Laboratories studying fusion events and other RNA-level alterations.

Established DNA Programs

Programs that want to preserve their current DNA assay while adding a separate RNA workflow.

Targeted NGS Workflows

Laboratories seeking focused RNA analysis as an alternative to broader RNA-sequencing approaches.

Request Information

Discuss Your RNA Fusion Testing Needs

Interested in adding standalone RNA fusion analysis to your existing DNA workflow?

Complete the form to request panel specifications, gene content, specimen requirements, pricing, or implementation information.

A Jant representative will contact you to discuss your laboratory’s current workflow and RNA testing needs.

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