Archer™ VARIANTPlex™ Lymphoma panel

产品详情

 

The Archer™ VARIANTPlex™ Lymphoma panel can 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.

 

 

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.

 

 

基因靶标

 

 

 

产品优势

 

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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.

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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.

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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.

 

 

产品资料

 

VARIANTPlex-LAC Protocol for Illumina

VARIANTPlex-HT Protocol for Illumina

VARIANTPlex Protocol for Illumina

VARIANTPlex Lymphoma Product Insert 

VARIANTPlex-HT Lymphoma Product Insert