NGS panel, cancer panel, targeted sequencing

WHAT WE OFFER

Extensive Predesigned and Customized Panel Services

CD Genomics is a full-service team for detection of gene variants. We have an advanced NGS sequencing platform and a wealth of experience in targeted sequencing and panel design.

Pan-Cancer Panel Sequencing

Targeted cancer panels focus on a select set of genes or gene regions that have known associations with cancer.

HBV/HPV/EBV Capture Sequencing

This approach determines low-abundance viruses by targeting gene conserved regions, providing valuable insights for medical research.

Medical Exome Panel

The deep coverage offered by targeted resequencing studies enables high sensitivity for rare variant calling.

Mitochondrial Diseases Panel Sequencing

Mitochondrial dysfunction research with NGS generates results using a single assay, in contrast to conventional methods.

Hereditary Cancer Panel Sequencing

Targeted panel sequencing provides more efficient and accurate targeting of specific genes or mutations in hereditary cancer-associated genes.

Bioinformatics Analysis

Customized analysis services combine affordable cost, optimized data processing capabilities, enhanced computational power, and many other advantages.