Run Sequence―Ion Torrent Next-Generation Sequencing Instruments
Ion Torrent next-generation sequencing (NGS) technology offers flexible sequencers and automation tools to help you find answers.
- A scalable platform
- Fast run times
- Easy to use with minimal hands-on time
Discover next-generation simplicity with integrated systems for speed and power. There is no faster or simpler way to harness the power of targeted NGS than with the Ion GeneStudio S5 Series systems and their plug-and-play consumables. When coupled with the Ion Chef System for library prep and templating, NGS automation is at your fingertips.
NGS systems and instruments
The Ion PGM Dx System is for in vitro diagnostic use. Read more ›
An NGS benchtop sequencer for your lab
Fast results. Flexible systems. Simple workflow.
- Results in a single day
- From sample to result
- Access challenging samples and sample types
- FFPE, fine needle aspirates, blood, tissue
- Supports changing needs in your lab
- Small and large projects on a single semi-conductor sequencer
- Conduct research across key applications
- Cancer research
- Complex diseases
- Microbial sequencing
Ion Torrent NGS systems for the work you do
|Human genetics research|
|DNA sequencing (targeted DNA panel or exome)|
|RNA sequencing (targeted RNA panel or transcriptome)|
|de novo sequencing|
* Cancer diagnostics available using the Ion PGM Dx System.
Ion Torrent NGS in practice—robust, repeatable performance
Ion Torrent NGS systems help deliver results on a national scale. Our systems were selected for The National Cancer Institute--Molecular Analysis for Therapy Choice (NCI-MATCH) trial in the United States, and for other large-scale clinical trials around the world.
NCI-MATCH trial active and approved sites
192 active sites
- 2/3 community hospitals
- 1/3 academic institutions
796 approved sites
Scalable and flexible platforms for focused next-generation sequencing applications.
Cost-effective platforms enable results
in a single day.
25+ years of global, industry-leading service and support for sequencing.
Platform cited by >4,000 publications, nationwide clinical trials.
For Research Use Only. Not for use in diagnostic procedures.