Discover important alterations for inherited disease research
Screen samples for genetic disease biomarkers with targeted NGS of 109 genes. Identify variants in all exons of CFTR, HBB, CYP21A2, and PAH, alterations in select intronic regions, and quantify SMN1/2 copy number.
Detect confidently with Archer VARIANTPlex NGS Panels for DNA.
Learn how the VARIANTPlex Expanded Carrier panel can identify key genetic alterations for your research.
Request a consultationSpecifications | |
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Targeted genes | 109 |
Genomic alterations | SNVs, indels, CNVs, ITDs |
Input nucleic acid required* | ≥10 ng |
Recommended number of reads | 1.5 M |
Hands-on time | <2.5 hours |
Total library prep time | 1.5 days |
Platform compatibility | Illumina® |
Reagent format | Lyophilized or liquid |
Supported sample types | Whole blood, saliva |
*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 Expanded Carrier panel can identify key genetic alterations for your research.
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