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.
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”
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.
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.
For Research Use Only. Not for use in diagnostic procedures.