Predesigned NGS Panel

CD-Genomics is a company with rich experience in targeted gene panel sequencing to accurately detect gene variations of interest.

CD-Genomics has an Illumina platform for variant detection. Multiple genes and regions of interest can be detected in a single assay. We have a series of predesigned panels that can be used directly to detect variants, saving time and money. Using targeted enrichment method, we can analyze single nucleotide variations (SNVs), insertions/deletions (indels), copy number variations (CNVs) and fusions with only 1 ng of DNA or RNA.

Gene Panel Workflow

CD Genomics provides the accurate and cost-effective targeted gene panel sequencing and bioinformatics analysis. Our professional expert team executes quality management, following every procedure to ensure confident and unbiased results. The general workflow for predesigned NGS panel sequencing is outlined below.

Predesigned NGS Panel

Features

For more information about the Predesigned NGS Panel or need other amplification requirements, please contact us.

Want to know more specific disease-related genes or just detect genes of interest? We offer Custom NGS Panel for you.

* For Research Use Only. Not for use in diagnostic procedures.

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  • 45-1 Ramsey Road, Shirley, NY 11967, USA
  • 1-631-275-3058 (USA)
           44-208-144-6005 (Europe)
  • 1-631-614-7828
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