Archer™ VARIANTPlex™ Lymphoma panel
Discover lymphoma insights with a targeted DNA panel
Detect single nucleotide variants, insertions, deletions, and copy number variations with targeted NGS of 51 genes relevant for B-cell and T-cell lymphoma research.
Detect confidently with Archer NGS Panels for DNA.
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Learn how the VARIANTPlex Lymphoma panel can identify key genomic alterations for your research.
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Panel specifications
| Specifications | |
|---|---|
| Targeted genes | 51 |
| Genomic alterations | SNVs, Indels, CNVs |
| Input nucleic acid required* | ≥10 ng |
| Recommended number of reads | 5 M |
| Hands-on time | <3.5 hours |
| Total library prep time | 1.5 days |
| Platform compatibility | Illumina® |
| Reagent format | Lyophilized or liquid |
| Supported sample types | Blood, bone marrow, fresh frozen, BMMC, PBMC, FFPE |
*Input mass requirements vary depending on type and quality. Unless the tumor cellularity and sample quality are high, 50 ng of FFPE-derived nucleic acid should be considered the minimum recommendation. If input is not limiting, 200 ng is recommended.
Gene targets
Interested in adding a few genes to this panel?
Customize this NGS panel by adding any of our functionally-tested designs or create a new panel that fits your exact requirements with Assay Marketplace.
Benefits
- Customizable content—Combine pre-designed panels, create, and easily add targets to your existing assay with Assay Marketplace, or work directly with a design expert.
- Detect confidently— Anchored Multiplex PCR (AMP™) chemistry is designed for compatibility with a wide range of sample types, including low-input and potentially degraded samples such as FFPE tissue. Archer Analysis includes a unique outlier detection algorithm that leverages position-specific data to enable variant detection even at low allele frequencies, empowering you to detect confidently.
- Achieve efficiency—Streamlined workflows for your lab are enabled by your choice of reaction-sized lyophilized reagents or high-throughput liquid reagents, while parallel workflows across all Archer panels provide efficient genomic characterization.
Ready to start?
Talk with our technical sales team. Learn how the VARIANTPlex Lymphoma panel can identify key genomic alterations for your research.
Request a consultationResources
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