A single platform for reliable genomic profiling

AMP is a 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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+603-7610 0388

Unit C109-110, Level 1, Block C,

Kelana Square,

17, Jalan SS7/26, Kelana Jaya,

47301 Petaling Jaya, Selangor, Malaysia.

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