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Maryville, Tennessee based Molecular Pathology Laboratory Network, Inc. (MPLN) Acquires the First FDA Approved High-Throughput DNA Sequencing Analyzer
Date:12/2/2013

Maryville, TN (PRWEB) December 02, 2013

Molecular Pathology Laboratory Network, Inc. (MPLN) announced today that it has acquired the Illumina MiSeqDx™, currently the only next generation sequencing system approved by the US Food and Drug Administration (FDA). MPLN will be the first laboratory in the country to own the FDA approved version of this revolutionary technology, and will leverage the system for the expansion of testing across all of its clinical laboratories including its clinical trials group Geneuity Clinical Research Services.

This exciting new technology is capable of screening numerous gene targets simultaneously at a fraction of today’s costs and does so with phenomenally high throughput. MPLN, a molecular reference laboratory specializing in Oncology, Women’s Health, and clinical research services, will utilize the Illumina MiSeqDx™ to offer physicians greater access to clinically actionable data at the gene level, and ultimately the facilitation of better patient outcomes.

“We are proud to soon host this revolutionary technology in-house and be the first lab in the country to offer such comprehensive DNA sequencing analysis,” said Dr. Roger Hubbard, MPLN Chief Executive Officer. “The Illumina MiSeqDx™ truly enhances our ability to offer the most comprehensive testing services personalized to the level of each person’s unique genetic make-up.”

About Molecular Pathology Laboratory Network, Inc.
Located in Maryville, Tennessee and with a branch laboratory in Richmond, Virginia, MPLN delivers an incomparable and unique client experience by offering the most comprehensive services and in
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