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Ready-to-Use NGS Panel

Ready-to-Use NGS Panel

By using amplicon-based approaches and hybridization capture-based approaches, CD Genomics has been developed a wide variety of different Read-to-Use NGS Panels to speed up your research process, which related to specific research applications, such as human cancer research, genetic disorders detection, infectious disease identification, etc. With the Read-to-Use NGS Panels, you can analyze single nucleotide variations (SNVs), insertions/deletions (indels), copy number variations (CNVs) and fusions with a small amount of DNA/RNA input, simultaneously saving time and money.

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Custom Panel

Custom Panel

Based on two targeted sequencing methods: amplicon-based approaches and hybridization capture-based approaches, CD Genomics can offer custom panel for the genes or regions you are interested in. The custom panels can provide a rapid, low-cost, ultra-sensitive, high throughput detection for single nucleotide variations (SNVs), insertions/deletions (indels), copy number variations (CNVs) or DNA methylation.

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Non-NGS Panel

Non-NGS Panel

CD Genomics' non-NGS panel Kits is based on highly sensitive qPCR assays that can detect low-frequency variants below 1% allele frequency. These Kits are ideals for genotyping and screening rare mutations in oncogenes and diseases. With the specific primers and fluorescent probes, these Kits enable to deliver high sensitivity and specificity results. CD Genomics’ non-NGS panel Kits provide a rapid, reproducible and affordable solution that employs a simple workflow and utilizes qPCR machines that are commonly used in research and clinical labs.

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

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  • 1-631-614-7828
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