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Comprehensive sequencing solutions

Choose from gold-standard Sanger sequencing technology and fragment analysis to flexible and scalable next-generation sequencing (NGS) to help your clinical research lab realize its full sequencing potential.

Choose Sanger sequencing to:

  • Study diseases with clearly defined phenotypes
  • Sequence 1 to 2 genes or up to 96 targets
  • Sequence 1–96 samples at a time without barcoding
  • Confirm NGS variants with up to 99.99% accuracy
  • Get longer read lengths (up to 1,000 bp)

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Choose NGS to:

  • Study diseases with higher levels of phenotypic heterogeneity
  • Sequence more than 2 genes or more than 96 targets
  • Sequence more than 96 samples for multiple targets
  • Discover novel variants

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Featured sequencing products

Sanger sequencing trade up, trade in, & upgrade

Trade in your 3100 Series Genetic Analyzer pic

Trade in your 3100 Series Genetic Analyzer for a new 3500 Series Genetic Analyzer at an incredible price.*

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Trade up your existing system to
better performance, higher
throughput and increased lab

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Upgrade data collection with special pricing for the latest versions of sequence analysis and fragment analysis software.*

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Sequencing technology & applications

Sequence from your benchtop with revolutionary "on-chip" technology.

Gold-standard technology—the ultimate sequencing verification tool.

Our portfolio supports a wide range of throughput and research application needs for DNA sequencing and fragment analysis.

Heritable genetic modifications that are not attributable to changes in the primary DNA sequence.

A detailed understanding of the RNA (coding and non-coding) in a given cell or cell sample is invaluable for understanding differential expression in normal and disease processes.

Manage and track genomic data for NGS or Sanger Sequencing in one platform.

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