AmpliSeq for Illumina products deliver a fast, highly multiplexed PCR-based workflow for amplicon sequencing using low-input DNA and RNA samples.

Use Ion AmpliSeq Designer, our free and easy yet powerful custom NGS panel design tool, to take your NGS testing in the direction you need.

nfcore/ampliseq is a bioinformatics analysis pipeline used for amplicon sequencing, supporting denoising of any amplicon and, currently, taxonomic assignment of 16S, ITS, CO1 and 18S amplicons. Phylogenetic placement is also possible.

With the Ion S5™ sequencers, Ion Chef™ System, and Ion AmpliSeq technology, you get the simplest targeted sequencing workflow that takes you from DNA to data with less than 45 minutes of total hands-on time.

Ion AmpliSeq is a targeted next-generation sequencing (NGS) technology developed by Thermo Fisher Scientific. It is designed to simplify and streamline the NGS workflow by enabling the amplification of specific genomic regions of interest.

Ion AmpliSeq HD technology is a new library amplification technology for Ion Torrent targeted next-generation sequencing (NGS) that gives you the power to design your own panels and find variants with very low limits of detection.

The AmpliSeq for Illumina Custom DNA Panel is the recommended replacement for the TruSeq Custom Amplicon and TruSeq Custom Amplicon Low-Input kits, which have been discontinued.

The AmpliSeq for Illumina Focus Panel is a targeted resequencing assay for biomarker analysis of 52 genes with known relevance to solid tumors. Using the Focus Panel, researchers can analyze both DNA and RNA concurrently.

Whether you’re interested in just a few targets or hundreds of targets, Ion AmpliSeq technology is flexible enough to suit your needs—use it with any genome across many research applications, from inherited disease to infectious diseases to oncology.

AmpliSeq for Illumina products deliver a fast, highly multiplexed PCR-based workflow for amplicon sequencing using low-input DNA and RNA samples.