Ion Torrent

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.

• Drug and companion diagnostic development
  
• Immune repertoire solutions
  
• Immuno-oncology solutions
  
• Liquid biopsy clinical research
  
• Targeted sequencing for oncology 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.

• Bacterial typing
• de novo microbial sequencing
• Metagenomics studies
• Microbial sequencing
  
• Viral typing

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.

• Gene expression profiling
  
• Methylation analysis
  
• Small RNA and miRNA sequencing
  
• Targeted DNA sequencing
  
• Targeted RNA sequencing
  
• Targeted transcriptome sequencing
  
• Whole-exome sequencing

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.

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.

• Small RNA and miRNA sequencing
  
• Targeted RNA sequencing
  
• Whole-transcriptome RNA-Seq

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.