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.



Targeted sequencing Gene Panels

GENEWIZ provides a variety of targeted resequencing panels, either pre-made or custom, that can cover any genes of interest or cancer-implicated genes.

Visit these pages to learn more about these services:

GENEWIZ also offers Sanger-based confirmatory sequencing to verify your final genes of interest.


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

In-house pipeline for optional Sanger-based confirmatory sequencing of final targets utilizing your NGS samples

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

Technical Resources

Blog | NGS, qPCR, or Sanger Sequencing: An Assay Selection Guide

This selection guide offers practical information about PCR + Sanger, qPCR, and NGS approaches to help you determine which assay best suits your project requirements, along with an interactive assay selection tool to aid your decision making.

NGS Platforms - Now with ILLUMINA Novaseq

Azenta is a certified service provider for Illumina NGS platforms and the PacBio Sequel. Please visit our NGS Platforms page for more information.

How To Order

Email | Phone 1-877-436-3949, Ext. 1