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AGENA @ AMP 2022

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Empowering Precision Medicine
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Advancement of PGx Testing: Development of Evidence-based Guidelines  More >

WELCOME
PGX WORKSHOP
ONCOLOGY WORKSHOP
SPEAKERS

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
View PDF

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


MINIMAL BIOINFORMATICS ANALYSIS

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


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.


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.


FLEXIBLE BIOMARKER DETECTION

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


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 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!
More

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.
More




ABOUT AGENA BIOSCIENCE

A global company with a mission to help laboratories translate genomic
discoveries into targeted, cost-effective testing.


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