Targeted Sequencing is an effective method for analyzing your selected gene(s) of interest by next generation sequencing. Whether you are interested in a few genes, or a few hundred genes, targeted resequencing panels offer high sensitivity and specificity, providing in-depth coverage, resulting in high-quality data.

With Custom Targeted Sequencing gene panels, you can discover point mutations, insertions/deletions (INDELs), copy number variations (CNVs), and gene rearrangements.




Discover genetic biomarkers associated with disease state
Characterize genetic associations to a particular phenotype, such as drug response
Genotype and classify eukaryotic and/or prokaryotic cell lines
Design genetic tests, such as for pharmacogenomics or oncology

Features & Benefits

Extensive multiplexing flexibility enables a more cost-effective assay

Dedicated, on-going support from experienced GENEWIZ scientists

Comprehensive bioinformatics options for robust downstream analysis

Availability of the most cutting-edge sequencing platforms

Workflow for Targeted Resequencing Panels

Extensive Quality Control is Performed at the Conclusion of Each Step of the Process
  • Experimental Design

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  • Targeting and Library Preparation

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  • Building


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  • Bioinformatics


Sample Submission Guidelines

GENEWIZ accepts the following sample types for targeted resequencing projects:

  • Purified genomic DNA
  • Frozen cell pellets (mammalian or bacterial)
  • PCR amplicons
  • Bacterial colonies
  • Formalin-fixed, paraffin-embedded (FFPE) thin sections (slides)
  • Select tissues
  • Blood
  • Swab

NGS Platforms

GENEWIZ is a certified service provider for Illumina NGS platforms. For information on our NGS platforms as well as recommended configurations for your projects, please visit the NGS Platforms page.

How To Order

Email | Phone (1-877-GENEWIZ (436-3949), Ext. 1) | Live Chat