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A single platform for reliable genomic profiling
AMP is robust for DNA and RNA sequencing that enables sensitive and specific detection of multiple mutation types. Build for MAXIMUM gene fusion detection targets both known and emerging genomic alterations molecular barcode enable advance error correction.
Liquid workflow can be complex and require master mixes
Simple, lyophilized reagents reduce the risk of contamination and save time
ARCHER
STANDARD NGS
Can miss rare or unknown fusions
Cannot discern starting molecule from PCR duplicates
PCR duplicates introduce errors, inflate true coverage and mask library complexity
Detects fusions regardless of partner
Uniquely tracks starting molecules prior to amplification
PCR duplicates are utilized for error correction to increase sensitivity and specificity
Sensitive fusion detection without prior knowledge of fusion partners
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