AmpliSeq for Illumina – a comprehensive targeted resequencing solution
Fast workflow and robust performance from a few to hundreds of genes, with as little as 1ng input
Expand Your Research Capabilities
Sequence with innovative NGS platforms that deliver exceptional data quality and accuracy, at any scale, with low hands-on time:
- Target variants for many applications with ready-to-use or custom panels
- Use a multiplexed, PCR-based workflow
- Transform data into insight with a variety of data analysis solutions
Sequence a Broad Range of Samples
AmpliSeq for Illumina is compatible with samples where available input quantity and quality are not limiting, such as blood, cell culture, or fresh-frozen tissues as well as challenging sample types, such as formalin-fixed paraffin-embedded (FFPE) tissue. The input requirement for DNA and RNA ranges from 1 ng to 100 ng, depending on the application needs. For most applications, we recommend 10 ng input per pool.
Prepare Libraries Quickly and Easily
Library preparation with AmpliSeq for Illumina is both fast and simple. Prepare an on-target, high-uniformity amplified library in as little as 5 hours with just 1.5 hours of hands-on time.
Analyze Hundreds of Genes at Once
AmpliSeq chemistry allows researchers to analyze hundreds of genes simultaneously with ultra-high multiplexed PCR with 12 to more than 24,000 amplicons in a single panel. Achieve complete coverage of large targets using multiple primer pools to create overlapping amplicons.