SeqCap EZ Developer


Product Overview

Targeting, enriching, and sequencing specific genomic regions of interest is key to advancing our knowledge of genomic variation and its relationship to disease. Researchers commonly use targeted resequencing to investigate causative mutations in disease associated regions, novel mutations present in disease, and to detect coding variants in genes.

Our designs have covered 100+ species with all major kingdoms covered for a broad variety of applications, including agriculture, forestry, fishery, evolution, environmental, metagenomics and more. Our list continues to grow.

Description Catalog Number Pack Size
SeqCap EZ Developer 06740278001 4 Reactions
SeqCap EZ Developer 06471684001 12 Reactions
SeqCap EZ Developer 06471706001 24 Reactions
SeqCap EZ Developer 06471714001 48 Reactions
SeqCap EZ Developer 06471722001 96 Reactions
SeqCap EZ Developer 06471749001 384 Reactions
SeqCap EZ Developer 06471757001 960 Reactions

Please Contact Us for ordering and questions

New! SeqCap EZ HyperCap Workflow User's Guide v1.0 

The SeqCap EZ system can now be used with the SeqCap EZ HyperCap Workflow. The HyperCap workflow provides an integrated, application-specific approach for efficient, streamlined and automatable targeted sequencing solution. It combines high-efficiency KAPA Hyper Prep and KAPA HyperPlus Library Preparation Kits with performance-optimized SeqCap EZ capture protocol.

For life science research only. Not for use in diagnostic procedures.

Product Description

SeqCap EZ Developer Kits enable enrichment of customer regions of interest up to 200 Mb for non-human genomes and unconventional human designs.


  • Apply our proven capture technology to unconventional genomes. Our superior target enrichment design algorithm is the foundation of our efficient capture - discover what uniform coverage and powerful enrichment can do for your genome research.
  • Simplify your bioinformatics pipeline with the experts you trust. Our expertise spans every taxonomic kingdom; let us create your custom design, with our experience from over 100 species. 
  • Maximize variant discovery while minimizing sequencing costs. Sequence more samples with your capacity using our efficient capture methods and multiplexing capabilities.

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