PCR was designed to amplify DNA, not prepare sequencing libraries.
PCR treats every sample the same, leading to data quality issues and requiring manual pre- and post-amplification quantification and normalization to yield balanced libraries.
Overamplification
Creates chimeras, duplicates, artifacts, and wasted reads.
Underamplification
Creates library dropouts and uneven pools.
Manual Normalization
Adds labor, cost, variability, and delays.
iconPCRTM was designed for NGS.
Instead of selecting an arbitrary cycle number and hoping every sample behaves similarly, iconPCR uses AutoNorm™ technology to monitor amplification in real time and automatically stops each reaction at the optimal endpoint for sequencing.
Overamplification
- Up to 4x fewer chimeras
- More usable reads
- Improved species detection
Faster Workflows
- 60% less hands-on time
- Fewer QC steps
- No manual normalization
Overamplification
- Up to 50% lower library prep costs
- Fewer re-runs due to dropouts
- Reduced sequencing waste
Trusted by leading genomics facilities
Validated across NGS applications
NGS technology agnostic
Sequencing-ready libraries for illumina, PacBio, Oxford Nanopore, and Element Biosciences instruments.
Low & variable input applications
Consistent results for single-cell, microbiome, cfDNA/liquid biopsy, and FFPE-extracted samples.
Scalable & automation-friendly
Available in 16- and 96-well formats. Compatible with liquid handlers and a variety of consumables.


