Archer™ VARIANTPlex™ Core Solid Tumor panel - 锚定多重PCR

产品详情

The Archer™ VARIANTPlex™ Core Solid Tumor panel can Efficiently detect single nucleotide variants, insertions and deletions, copy number variations, and microsatellite instability with targeted NGS of 60 genes relevant for colorectal, breast, melanoma, pancreatic, NSCLC, and other cancer research.

	Specifications
Targeted genes	60
Genomic alterations	SNVs, indels, CNVs, ITDs, MSI
Input nucleic acid required*	≥10 ng
Recommended number of reads	4.5 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	FFPE, fresh frozen, cytology smear, FNA

*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

●	Detect confidently—A unique outlier detection algorithm leverages position-specific data to enable variant detection even at low allele frequencies, one of the many ways that Archer Analysis empowers you to detect confidently.
●	Detect confidently—A unique outlier detection algorithm leverages position-specific data to enable variant detection even at low allele frequencies, one of the many ways that Archer Analysis empowers you to detect confidently.
●	Achieve efficiency—Streamlined workflows for your lab are enabled by choice of reaction-sized lyophilized reagents or high-throughput liquid reagents, while parallel workflows across all Archer panels provide efficient genomic characterization.
●	Customize content—Use Assay Marketplace to modify any panel to fit your lab's needs or start from scratch to keep up with the pace of discovery.

产品资料

VARIANTPlex-HT Protocol for Illumina

VARIANTPlex HS-HGC Protocol for Illumina

VARIANTPlex-HT Core Solid Tumor Panel Product Insert

VARIANTPlex Core Solid Tumor Product Insert