1-631-338-8059 info@cd-genomics.com

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.

Amplicon sequencing: 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-based target enrichment: 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.

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.

* For research purposes only, not intended for clinical diagnosis, treatment, or individual health assessments.