CE-IVD Marked Next-Generation Sequencing System
The platform’s automated workflow minimises user intervention and the potential for human error.
The system enables users to perform both diagnostic testing and clinical research on a single instrument.
The system enables users to perform both diagnostic testing and clinical research on a single instrument.

Laboratory products

CE-IVD Marked Next-Generation Sequencing System

05 Apr, 2022

Published over 4 years ago. See the latest and most current information on Laboratory products.

Instrument for rapid NGS in diagnostic applications and clinical research 

The CE-IVD marked Ion Torrent Genexus Dx Integrated Sequencer from Thermo Fisher Scientific, is an automated, next-generation sequencing (NGS) platform that delivers results in as little as a day. Designed for use in clinical laboratories, the fully validated system enables users to perform both diagnostic testing and clinical research on a single instrument.

“Next-generation sequencing has become an essential tool to bring the promise of precision medicine therapies to patients. With the automated, easy-to-use Genexus Dx Integrated Sequencer, any hospital - including regional and community hospitals - can bring NGS in-house, giving clinicians access to timely, comprehensive genomic profiling results,” said Garret Hampton, President, Clinical Next-generation Sequencing and Oncology at Thermo Fisher Scientific. “With faster answers, the results can aid clinicians in their patient management decision making which may include therapeutic options.”

In support of increasing physicians’ access to rapid NGS results, Thermo Fisher is also developing a complete sample-to-report diagnostic workflow and a portfolio of clinically validated assays, including those for comprehensive genomic profiling and haemato-oncology, on the Genexus System.

 Thermo Fisher introduced the Ion Torrent Genexus System for research use only in 2019 as the first fully integrated NGS platform that delivers results in as little as 24 hours. The platform’s automated workflow minimises user intervention and the potential for human error, making NGS accessible for all labs.

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