Discover lymphoma insights with a targeted DNA panel
Detect single nucleotide variants, insertions, deletions, and copy number variations with targeted NGS of 49 genes relevant for B-cell and T-cell lymphoma research.
Detect confidently with Archer NGS Panels for DNA.
Learn how the VARIANTPlex Lymphoma panel can identify key genomic alterations for your research.
Request a consultationSpecifications | |
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Targeted genes | 49 |
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.
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.
Talk with our technical sales team. Learn how the VARIANTPlex Lymphoma panel can identify key genomic alterations for your research.
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