AmpliSeq for Illumina Exome Panel

The AmpliSeq for Illumina Exome Panel brings the speed and simplicity of PCR to exome sequencing, enabling researchers to sequence eight exomes in a single run and identify germline variants in less time. Key features include:

Fast exome library preparation

• Prepare 8 exome libraries in < 7.5 hours with < 1.5 hours hands-on time

Comprehensive coverage

• Access uniform and specific coverage; includes >97% of the Consensus Coding Sequences (CCDS) annotation

Accurate Data

• Detect common single nucleotide variants (SNVs), copy number variants (CNVs), and small indels

The Exome Panel is part of an integrated workflow that includes AmpliSeq for Illumina polymerase chain reaction (PCR)-based library preparation, Illumina sequencing by synthesis (SBS) next-generation sequencing (NGS) technology, and automated analysis.

This ready-to-use panel saves you the time and effort of identifying targets, designing primers, and optimizing panels.

Learn More About AmpliSeq for Illumina