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Ion Torrenrt - Genexus System Automates Sample and Library Preparation
The Ion Torrent Genexus System automates sample and library preparation, sequencing, analysis, and reporting. The Genexus Purification System and Genexus Integrated Sequencer with Genexus Software work together seamlessly, tracking sample information and results automatically through the process. This automated system reduces manual steps and facilitates quality data and quick reports.
Automated NGS is performed by the Genexus Integrated Sequencer and Genexus Purification System. See the instruments performing a sample-to-result assay or schedule a tour through the interactive demo of the instruments.
The end-to-end NGS workflow is performed by the Genexus System completing and automating NGS steps. The Genexus Purification System replaces sample prep by extracting and quantifying nucleic acids in about two or four hours. The Genexus Integrated Sequencer automates library prep, templating, and sequencing. The one ecosystem software links instruments to report and has been simplified for a lower learning curve. Data files can be exported for third party analytics or use Thermo Fisher analytic tools to generate customizable report formats based on guidelines, clinical trials, curated markers, and novel variants.
Oncomine Solutions used with the Genexus System provide a complete NGS testing workflow from sample-to-report. The time to complete the workflow is comparable to other methods including IHC yet provides full genomic profiling. Multiple Oncomine assays are available on the Genexus System to assay key biomarkers found in multiple cancers.
Oncomine assays for a range of research applications:
- Genomic profiling
- Liquid biopsies
- Hematological malignancies
- Immuno-oncology
Infectious disease research solutions
Ion Torrent NGS technology is based on ultra-high-multiplex PCR, the same technology that has enabled public health agencies to closely monitor viral infections. This includes assays to complete viral genome sequencing and variant identification.
Application: inherited disease
Studying heritable diseases can be challenging. Ion AmpliSeq On-Demand panels allow you to build custom panels from over 5,000 pretested genes that are most relevant in research on inherited diseases, including hereditary cancer, primary immunodeficiency, hearing loss, muscular dystrophy, and more. This is a simplified method to bring NGS into a laboratory.
Application: design your own panels
The Ion AmpliSeq Designer helps you obtain custom assays with minimal time and effort. This web tool leads you through the steps and choices to build custom primer panels.