One platform. Endless potential.
Archer Analysis is a versatile bioinformatics platform that automates processing of sequencing data generated from all Archer next-generation sequencing (NGS) assays. The analysis pipeline produces highly confident gene mutation detection from RNA, DNA and ctDNA sources. The simple user interface paired with in-line visualization enables powerful and clear reporting. Since Archer Analysis allows for third party integration and deploys securely to the cloud or on a server, it will fit within your lab infrastructure.
Known and Novel Fusion Detection
Anchored Multiplex PCR (AMP™) chemistry is built for gene fusion detection, permitting amplification of both known and unexpected genomic regions of interest. Results are cross-checked against the Archer Quiver® Fusion Database to indicate novel fusions or those found in the literature.
Sensitive and specific variant detection
Molecular Barcode (MBC) adapters are used to count unique molecules and characterize sequencer noise, revealing mutations below standard NGS-based detection thresholds. Through advanced MBC-based statistical support, Archer Analysis sets a new standard in extreme sensitivity and specificity.
Quantitative CNV detection
MBCs enable unique molecule counting to provide robust copy number analysis in DNA. Powerful visualization tools in Archer Analysis give you critical information about your sample.
The CNV visualization tool in Archer Analysis allows users to easily visualize copy gains and losses with exon-level resolution and track CNVs within your own database. The tool is dynamic, interactive and has customizable sensitivity settings.
Safe and Secure
Analysis Unlimited, the cloud-based configuration of Archer Analysis, is third party verified HIPAA compliant, ensuring that all data remains protected and private at all times.