Each kit generates target-enriched cDNA libraries from RNA, even from FFPE samples. Produced libraries can be analyzed, free of charge, with Archer Analysis, an optimized in silico bioinformatics solution that clearly presents detected fusions, breakpoints and variants with robust statistical quality assurances. Each platform-specific kit contains all the primers, enzymes and buffers needed to prepare your target-specific library from input nucleic acid. The lyophilized enzymes and buffers for each step are aliquoted into color-coded 8-tube strips, and the tubes for each step are individually wrapped in mylar bags for maximum stability, minimal sample cross-contamination and rapid library preparation.
Molecular Barcode Adapters are required and supplied separately for multiplexing and sample-tracking flexibility.
FOR RESEARCH USE ONLY. Not for use in diagnostic procedures.
Comprehensive and disease-specific NGS panels to detect known and novel fusions in blood cancers
Oncology Research Panel
Detect 75 gene fusion targets and any known and unknown fusion partners with this comprehensive NGS based assay.
NGS target-enrichment kit to detect gene fusions, SNVs and indels in 31 thyroid and lung cancer-implicated genes
Characterize fusions and mutations of over 50 genes linked to various solid tumors, including carcinomas, sarcomas and lymphomas.
ALK RET ROS
Detect and identify fusions and mutations of human ALK, RET and ROS1 genes, including mutations involved in crizotinib resistance.
Locate and characterize fusion partners of 26 genes associated with these soft tissue cancers using this NGS-based assay.
Archer Custom Panels
Bundle your preferred genes and exons with our simple lyophilized workflow, fusion detection technology and comprehensive analysis pipeline.
These half-functional universal adapters are at the center of the FusionPlex workflow and include primer-binding, index and barcode sequences necessary for:
Archer® SureShot™ ALK RET ROS1 fusion-positive and -negative controls are formalin-fixed, paraffin-embedded (FFPE) curls of homogeneously mixed, genetically defined cell lines.Archer® SureShot™
The Archer FusionPlex Assay system generates target-enriched cDNA libraries for next-generation sequencing (NGS). The system leverages Anchored Multiplex PCR (AMP™) to selectively amplify cDNAs of specific genes of interest in a sample along with any fusion partners, known or unknown.
The libraries are ready for single sample or multiplex sequencing on Illumina® or Ion Torrent™ next-generation sequencing platforms. The sequencing data is then analyzed using Archer Analysis to detect true positive calls for gene fusions (both known and unknown), isoforms, insertions/deletions (indels) and single nucleotide variants.
And the FusionPlex system can do this with as little as 20ng input nucleic acid from FFPE samples.
Archer FusionPlex Assays are powered by powerful Anchored MultiPlex PCR (AMP) technology. Unlike traditional opposing primer-based library preparation techniques, AMP utilizes random start sites to generate greater library diversity and attain target recovery of short fragments.
All FusionPlex Kits include platform-specific reagents and lyophilized enzymes and take 3.5 hours hands-on time and 8 hours total preparation.
Archer Analysis is a complementary software suite that provides in-depth sequencing data analysis and interpretation. Archer Analysis was designed for secure data analysis and reporting. The software is available as a free download comprised of a fully contained set of virtual machine images that are installed on your servers, so proprietary or confidential information remains securely behind your firewall.
RNA is better for fusion detection than hybrid capture
AMP is better for novel fusion detection
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