Ready-to-Use NGS Panel

Brief Introduction

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.

• Multiplex Amplicon Sequencing panel: Specific primers are designed for PCR amplification for the target region of interest, multiplex up to 20,000+ amplicons in each reaction. Sequencing adapters are ligated or added by a second PCR amplification and the targeted DNA library is constructed. High-throughput sequencing is then performed.
• Hybridization Capture panel: Based on the principle of base complementary pairing, nucleic acid probes are designed for specific regions of the genome of interest. The target region hybridization enrichment of DNA/RNA library is carried out based on liquid phase environment, and the specific genetic mutation or somatic mutation in the target region are detected by high-throughput sequencing technology.
• Methylation Hybridization Capture Panel: This solution enables comprehensive, targeted detection of key CpG islands and CpG sites. Using an advanced methylation probe design, it ensures accurate assessment of methylation levels across diverse sample types. By delivering higher sequencing depth at a cost-effective scale, it substantially improves detection sensitivity and accuracy.

Features

• Fast and streamlined workflow enables library construction in just a few hours.
• All Kit components are subjected to stringent quality control ensuring the consistency and reproducibility of library preparation.
• Optimized to deliver high specificity and highly uniform sequencing results.
• Low-frequency variants can be detected with just a small amount of DNA/RNA input.

For more information about Read-to-Use NGS Panel or need other requirements, please contact us.