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, and agrigenomics.
Any application. Any research question.
Introducing the Ion GeneStudio S5 Series
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.
Transcriptome sequencing, or RNA sequencing (RNA-Seq), provides fundamental insights into how genomes are organized and regulated. RNA sequencing relies on next-generation sequencing (NGS) methodology and techniques.
Copy number variation (CNV) analysis is a next-generation sequencing method that can be used to analyze chromosomal aberrations like aneuploidy. Next-generation sequencing on the Ion GeneStudio S5 Systems offer a simple, rapid technique that is designed to reliably deliver easy-to-interpret data.
Ion AmpliSeq technology, combined with accessible Ion Torrent next-generation sequencing, enables any lab to see and discover more with small RNA sequencing.
The Ion PGM or Ion GeneStudio S5 Systems enable rapid and affordable viral typing research during disease surveillance, using archived samples from outbreak investigations and disease etiology studies.
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 on the Ion GeneStudio S5 systems.
With its increased throughput, higher accuracy, and longer reads, the Ion GeneStudio S5 Systems can be used for analyzing retrospective samples for specific disease types, surveillance, investigating outbreaks, and determining disease etiology.
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.
Ion Torrent semiconductor sequencing has revolutionized de novo sequencing for microbial research, providing a simple, low cost system that delivers accurate results in a day.
The Ion PGM and Ion GeneStudio S5 Systems provides rapid, low-cost complete-genome sequence information by using hundreds to thousands of genes for typing research, enabling higher discrimination and more accurate typing of individual strains.
For Research Use Only. Not for use in diagnostic procedures.