(203) 208-3464 info@wrenlaboratories.com
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About Wren

Transforming cancer diagnostics through liquid biopsy mRNA.

Focused on molecular liquid biopsy cancer diagnostics since 2014 — a commercial extension of decades of academic and medical research into non-invasive tests for cancer and other diseases.

Our mission

Transform cancer diagnostics through innovative liquid biopsy mRNA technology.

Wren Laboratories is a CLIA, CAP, NYSDOH and ISO 15189-certified clinical testing and R&D laboratory established in 2014.

Our mission is to pioneer innovative in vitro diagnostics using machine learning and liquid biopsy-RNA technologies — enhancing detection of minimal residual disease, predicting and monitoring cancer response to therapies, and improving prognosis and outcomes.

Our values

Science, innovation and collaboration.

Be it blood or saliva, our molecular cancer diagnostics provide actionable disease information in real time.

Committed to science

Scientific discipline and the benefits of rigorously applied molecular science.

A pioneering spirit

Combating cancer effectively demands an innovative approach and cutting-edge techniques.

True collaborators

Managing cancer requires inspired teamwork. We are open, connected and fully collaborative.

Excellence in execution

Across research, clinical testing and data analysis.

Focused on success

The stakes could not be higher; our principal focus is positively impacting the lives of cancer patients.

Credentials & licenses

Certified to the highest standards.

Every test is performed in our accredited clinical laboratory in Branford, Connecticut.

CLIA certification07D2081388
CAP accreditation8640840
NYSDOH-CLEP licensePFI: 9138
Connecticut licenseCL-996
California licenseCDS-00800634
ISO 15189 certificate8640840
Wren Laboratories clinical laboratory
About our lab

CAP-accredited. CLIA-certified.

All molecular research, testing and analysis is conducted at our clinical laboratory in Branford, CT. Most of our liquid biopsy tests use real-time quantitative PCR (qPCR) on RNA isolated from peripheral blood or saliva — known for sensitive, specific and reproducible gene-expression measurement.

Our experienced, highly trained technicians follow extensive quality-control procedures at every stage:

RNA quantity & quality

Sufficient purified RNA for all reactions, meeting purity criteria including checks for excess genomic DNA.

Gene-specific ranges

Each gene product’s measured quantity must fall within established ranges.

Efficiency of qPCR

Amplification, doubling target each cycle, must fall within defined limits.

Accuracy & precision

Each gene tested must meet established accuracy and precision specifications.

Strategy & pipeline

Our scientific strategy and forward focus.

We identify gene signatures that categorize the state of a disease — primarily cancer — to identify recurrence in time or assess whether therapy is working.

Algorithms

Biomathematical algorithms identify gene-signaling clusters that reveal tumor proliferation and metastatic potential.

mRNA

First identification of circulating neuroendocrine and other tumor-cell mRNAs — signatures that detect disease missed by standard of care, and predict growth, metastasis and therapy sensitivity.

Beyond NETs

Blood biomarkers for prostate cancer (PROSTest), prediction of PRRT response (PPQ), and saliva-based PCR tests for different cancers.

Pipeline

Diagnostics in development for breast, colon, lung, melanoma, myeloma and pancreatic cancer — and non-cancer diseases such as endometriosis.

Get started

Providers, order your test here

Order NETest 2.0® or PROSTest® through our portal or with the requisition form — kits ship directly to your office.