Description
Overview
Create amplicon panels with the genes you want. AmpliSeq for Illumina On Demand panels provide a choice of > 5000 pretested genes with known content relevant for inherited disease research, including hereditary cancer, primary immunodeficiency, hearing loss, and muscular dystrophy.
AmpliSeq chemistry and Illumina next-generation sequencing (NGS) technology provide unmatched data quality, even from low-quality starting materials such as formalin-fixed, paraffin-embedded (FFPE) tissues.
Choice of > 5000 pretested genes
Easy online ordering - Use DesignStudio Software, a free, user-friendly tool, to create panels optimized for your genomic content of interest.
Convenient small pack sizes - On-demand panels are available for 1 (24 amplicons) to 500 (15,000 amplicons) genes and are offered in small pack sizes of 24 and 96 reactions.
What accessories do I need?
AmpliSeq for Illumina Direct FFPE DNA is strongly recommended for FFPE samples. The AmpliSeq for Illumina Sample ID Panel is an optional accessory to facilitate sample management.
Example workflow
DesignStudio Software
AmpliSeq for Illumina Library PLUS
AmpliSeq for Illumina On-Demand
AmpliSeq for Illumina CD Indexes
iSeq 100 System
MiniSeq System
MiSeq System
NextSeq System
BaseSpace Sequence Hub DNA Amplicon App
Local Run Manager RNA Amplicon Module
BaseSpace Variant Interpreter
Related applications and methods
AmpliSeq for Illumina On-Demand Panels
Create amplicon panels with the genes you want. Select from a catalog of pretested genes with known content relevant for inherited disease research.
Cancer Genomics Research
Our sequencing and microarray technologies support a broad range of cancer genomics research applications, from DNA to RNA analysis, epigenetics, and more.