Sequencing Panels for Academic and Clinical Research
Targeted gene sequencing is now easier than ever.
AmpliSeq for Illumina ready-to-use panels for cancer research include curated genes with demonstrated relevance in cancer. Panels include multiple amplicon sizes and can be used with various targets and sample types, including formalin-fixed, paraffin-embedded (FFPE) DNA, without requiring additional purification steps.
High Accuracy
Illumina next-generation sequencing (NGS) systems have generated 90% of the world’s sequencing data† and have been cited in more than 26,000 publications. With > 90% on-target reads and > 93% coverage uniformity, our instruments deliver the accuracy you need for reliable variant detection. AmpliSeq for Illumina panels are stringently tested and analytically validated, so you can be confident in your sequencing data.
Lab Efficiency at Any Scale
The AmpliSeq for Illumina workflow offers a fast, scalable, and cost-effective sequencing solution for Illumina systems. Unlike qPCR or Sanger sequencing, which require iterative testing, these comprehensive gene panels allow you to analyze many potentially causative genes in a single assay.
Looking to request a quote, choose a panel, or ask a question about AmpliSeq for Illumina products? We can help.
AmpliSeq for Illumina Ready-to-Use Cancer Panels
For a limited time, you can save 50% the first time you order any of the following AmpliSeq for Illumina panels by entering code ASVLD50OFF at checkout when you order online.* Try an AmpliSeq for Illumina panel today and see how easy sequencing can be.
AmpliSeq for Illumina Focus Panel
Targeted DNA and RNA research panel investigating 52 genes with known relevance to solid tumors. This ready-to-use panel is available alone or as part of a bundle, which includes the AmpliSeq for Illumina Focus Panel, library prep reagents, index adapters, and the MiSeq Reagent Kit v2 for additional savings and convenience.
AmpliSeq for Illumina Cancer Hotspot Panel v2
Targeted research panel investigating ~2800 COSMIC mutations from 50 oncogenes and tumor suppressor genes.
AmpliSeq for Illumina BRCA Panel
Targeted research panel investigating somatic and germline variants in BRCA1 and BRCA2.
AmpliSeq for Illumina Comprehensive Panel v3
Targeted DNA and RNA research panel investigating variants across 161 cancer-associated genes, including kinase domains and genes involved in DNA repair.
AmpliSeq for Illumina Myeloid Panel
Targeted panel to investigate 40 DNA genes, 29 RNA fusion driver genes, and 5 gene expression levels associated with myeloid cancers.
Don’t see the panel you need?
Getting Started
It’s easy to get started with AmpliSeq for Illumina panels. Illumina experts are available to help you through entire workflow, from library prep to data analysis.
Transitioning to AmpliSeq for Illumina on the iSeq 100 System
Switching to a new NGS workflow requires careful planning. For each step of the process, you’ll find key questions and answers to help you get started with AmpliSeq for Illumina panels on the iSeq 100 System.
Transitioning from TruSeq Custom Amplicon to AmpliSeq for Illumina
Interested in switching your existing TruSeq Custom Amplicon experiments to the AmpliSeq for Illumina Custom DNA Panel? Find experimental considerations, support resources, and tips and tricks from both Illumina experts and fellow TruSeq Custom Amplicon users.
* Promotion is valid for one-time use only. It may be used on a single order for up to 96 reactions.
Terms and Conditions
† Data calculations on file. Illumina, Inc., 2017.