VISIT US AT AMP 2022 - BOOTH  #713

Enabling Clinical Laboratories to Deliver Targeted Genomic Testing
Agena Bioscience enables laboratories to deliver affordable targeted genetic testing in diverse fields such as cancer profiling for solid tumors and liquid biopsies, inherited genetic disease testing, pharmacogenetics, and clinical research. Learn more at the upcoming Association for Molecular Pathology (AMP) Annual Meeting & Expo, booth #713, on November 1-5, 2022, in Phoenix, AZ. 
MassARRAY System Brochure
MassARRAY® System Brochure
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Watch the video below to see why laboratories rely on the MassARRAY for accurate, cost-efficient targeted results.

MassARRAY Video | Why Laboratories Choose the MassARRAY System

Bioinformatics

Minimal Bioinformatics Analysis

Simplify data analysis by targeting only relevant mutations, unlike other extensive approaches such as sequencing. No bioinformatics team needed!
Simple Workflow

Simple Workflow

Combining automation, minimal hands-on time and onboard data analysis, the MassARRAY System utilizes a simple and fast workflow and delivers a suite of applications.
Multiplexing Range

Broad Multiplexing Range

Target up to 50 DNA variants in a single PCR reaction and process up to 96 or 384 reactions on a single SpectroCHIP® Array, and test hundreds of mutations in a single workflow.
Panels

Flexible Biomarker Detection

Detect SNPs, insertions, deletions, translocations, copy number variations, and methylation markers with one system.
Productivity

Maximum Productivity

Sample to results in a single day. Run up to eight 96-well or six 384-well plates in a full workday with the flexibility to process two more plates overnight.
Cost Effective

Cost-Effective Testing

Multiplexed analysis plus the elimination of fluorescent markers allows for the lowest price per sample.
Connect with Us
Great news! If you missed our recent PGx webinar about predictive biomarker identification, you can view it on demand. Find out about the latest evidence supporting predictive biomarkers and how drug efficacy and safety are related to PGx variability. View the webinar now!
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The more touchpoints along a specimen's journey increase the chance for errors, especially with NGS workflow. Our sample identification solutions use single nucleotide polymorphism (SNPs) detection to provide a unique genetic fingerprint for each sample throughout the testing journey.
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