NGS Library Prep
Without the Normalization Bottleneck

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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

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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.

Ready to experience consistent quality across 96 samples in a single run?
Contact us today.

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