Ion Torrent next-generation sequencing
Next-generation sequencing (NGS) utilizes massively parallel sequencing to generate thousands of megabases of sequence information per day, opening doors to new research studies that were once difficult to accomplish in a practical manner. Powered by semiconductor chips, Ion Torrent next-generation sequencing technology helps you implement a fast and simple workflow that scales to your research needs across multiple applications including inherited diseases, oncology, infectious diseases, reproductive genomics, human identification, agrigenomics and more.
Ion Torrent next-generation sequencing systems
Scalable targeted NGS to support small and large projects?
The Ion GeneStudio S5 system is a scalable, targeted-NGS workhorse with wide application breadth and throughput capability.
Specimen to report in a single day with a hands-off, automated workflow*?
The Genexus System is the first turnkey NGS solution that automates the specimen-to-report workflow and delivers results in a single day with just two user touchpoints.*?
Enabling NGS analysis and discovery of multi-biomarker types (fusions, insertion/deletions (indels), single nucleotide variants, and copy number variations), Oncomine assays are part of an end-to-end workflow that includes simple, scalable sequencing with optimized bioinformatics and reporting—designed for cancer research.
Uncover microbial diversity, study pathogen outbreaks, and identify mutations that may be associated with antibiotic resistance. Take advantage of increased throughput, higher accuracy, and longer reads to produce rapid and accurate sequencing of microbes with streamlined sample preparation and a simple, scalable, and optimized data analysis workflow.
Our complete NGS solutions are uniquely suited to research in understanding how the combination of genetics and the environment influence development of complex diseases such as autoimmune disorders, neurodegenerative diseases, and many others.
Copy number variation (CNV) analysis is a next-generation sequencing method that can be used to analyze chromosomal aberrations like aneuploidy. Ion Torrent targeted NGS is a simple, rapid technique that is designed to reliably deliver easy-to-interpret data.
Adopting targeted NGS for forensic DNA analysis and phenotyping in your laboratory is simpler than ever when you combine the Ion Chef System and Ion GeneStudio S5 Systems with optimized Precision ID library preparation, template preparation and sequencing kits, and forensically relevant panels.
Uncover traits to drive breeding decisions and help address the challenges of feeding a growing global population. Our instruments, reagents, and solutions for plant and animal genotyping applications enable simple, scalable, and affordable NGS that can help you drive remarkable agricultural innovations.
Targeted sequencing is a rapid and cost-effective alternative to whole genome sequencing. Ion AmpliSeq technology transforms this application by enabling researchers to rapidly and simply amplify thousands of targets using as little as 1 ng of DNA.
Human genetic variation is present in many different forms in the genome, ranging from large, structural, chromosomal changes to single nucleotide polymorphisms (SNPs). We offer a broad range of products for analysis of genetic variation and genomic profiling.
Exome sequencing is a targeted sequencing approach that interrogates only the disease-causing exonic regions of the genome. We enable flexible, and simple exome sequencing.
*Specimen-to-report workflow will be available after the Ion Torrent Genexus Purification System and integrated reporting capabilities are added in 2020.
For Research Use Only. Not for use in diagnostic procedures.