Offering the expanding range of sequencing services available today, with applications in human, plant , animal, and microbial research, we can provide innovative, affordable, and reliable solutions for virtually any genomic challenge our customers and collaborators.
The mission of the CD Genomics is to facilitate interdisciplinary genomics research by providing researchers access to cutting-edge technologies in the field of genomics.
Support all types of genomic research:
Our facilities are featured by next generation sequencing(NGS) and Sanger sequencing technologies, providing the high throughput sequencing capacity. We ascribe to the highest standards in genomics solutions for sample preparation, sequencing experiment design, and customized bioinformatics analysis, providing fast, accurate, and reliable sequencing services.
Our genomics solutions include:

·         de novo Sequencing: Sequencers and data analysis solutions facilitate de novo sequencing and assembly of novel genomes.

·         Whole Genome Resequencing & Human Whole Genome Sequencing: Whole genome resequencing characterize the genetic diversity within the organism's species or between closely related species, detect the full range of genetic variation such as SNPs, insertions, deletions, inversions, complex rearrangements, and copy number variation.

·         Exome and Target Region Sequencing: Current approaches become cost-prohibitive when working with large numbers of samples and regions, or demonstrate variable coverage. Exome sequencing and Targeted resequencing overcome these challenges.

·         Whole Genome Mapping: You will be able to investigate microbial structure, function, diversity and genetics, without the need for amplification, PCR, cloning, paired-end libraries, pure isolates, or genomic specific reagents.

·         Human MHC-Seq: This new technology can type 26 HLA genes with 4-digit resolution and detect variants such as SNPs and InDels.