CD Genomics is a company with rich experience in panel design and in-silico optimization. By using amplicon-based approaches and hybridization capture-based approaches, CD Genomics has been developed a wide variety of 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.
CD-Genomics' Read-to-Use NGS Panels are compatible with Illumina platform for variant detection. Multiple genes and regions of interest can be detected in a single assay. If the content already meets your need, you can order the panels now, saving time and money.
For more information about Read-to-Use NGS Panel or need other requirements, please contact us.