Ion AmpliSeq NGS Panels for Targeted Sequencing

When analyzing suspected variants in genetic diseases, you may need a discovery tool that is both rapid and cost-effective for analyzing multiple genes. 

Ion AmpliSeq™ panels enable high-throughput analysis of many genes using next-generation sequencing (NGS), and can help detect multiple mutation types (SNPs, indels and copy number variants) in a single panel. 

See how Ion AmpliSeq™ technology works ›

Dr. Janet Chou and other clinical researchers at Boston Children’s Hospital improve variant yields and get faster results by adopting targeted gene panels in their lab versus outsourcing whole-exome sequencing.

“Applications of targeted NGS panels for clinical research of primary immunodeficiency diseases”

 Watch webinar ›

The Department of Neuromuscular Research at the National Center of Neurology and Psychiatry (NCNP) in Japan adopted Ion AmpliSeq panels as a first-line mutation discovery tool and found the variant yield and cost per sample to be better than the traditional Sanger sequencing-MLPA workflow.

Read more ›

The convenient predesigned panels allow researchers to focus on data generation and analysis, not on the labor-intensive primer design and target selection steps.

Our community panels are designed with input from leading researchers in the scientific community.

If the Ion AmpliSeq ready-to-use panels don't match your gene targets, then simply select a subset of the targets or enter your specific genomic content online, and we will design and create customized Ion AmpliSeq NGS panels just for you.