“ Unlike Whole Genome Sequencing,
Targeted Sequencing is a technique that selectively analyzes specific regional sequences of genomes.”
Our Target Enrichment Panel uses hybridization-based capture technology to enable the core
process of Target Sequencing, which is the separation and analysis of specific regional sequences of
entire genomes. It is also able to accurately analyze all types of mutations, such as SNV, InDel CNV,
Celemics Target Enrichment Panel utilizes our intrinsic probe design, rebalancing, and molecular
barcode technologies to efficiently analyze not only hard-to-capture areas such as GC-rich and
homologous regions but also samples originating from circulating tumor DNA and FFPE with extremely
small amounts of damaged DNA and RNA as well. We also provide our proprietary functionalities
to prevent sample cross-contamination.
For all Customized and Ready-to-Use Panels, Celemics uses standard DNA samples to run product QC for wet-lab tests, NGS runs, and bioinformatics up to the standard of the actual product used by our clients, and also provide detailed QC information as well.
Through this process, we can reduce both the possibility of experimental failure and the time and costs involved with our clients evaluating the products themselves. Additionally, through our proprietary 2-step mass production technology, we can manufacture high-quality reproducible customized panels, which makes first-time-user clients have their subsequent orders.
Celemics Target Enrichment Panel is compatible with all currently available NGS equipment, such as Illumina, Thermo Fisher Scientific, Pacific Bioscience, and MGI, and provides bioinformatics software for data analysis.