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CD Genomics-the genomics service company
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Genomics Sequencing

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Equipped with advanced NGS platforms, state-of-the-art technologies, and coupled with specialized scientists, CD Genomics delivers a broad array of genomic solutions to meet your diverse research goals and budgets.

Next-generation sequencing (NGS) technologies have demonstrated the capacity to sequence DNA at unprecedented speed, and has made a striking impact on genomic research. By sequencing the whole human genome, people are able to unravel the complexity of the human genome in terms of genetic variations. As an effective alternative strategy to whole genome sequencing, whole exome sequencing (WES) is a powerful and cost-effective way to get deep insight into the disease-associated variations. For research only on the regions of interest, target sequencing provides ultra-high resolution of the selected regions, which lays significant foundations for variations detection.

Genomics Sequencing

We ascribe to the highest standards in complete genomics solutions for sequencing experiment design, target enrichment library construction, and customized bioinformatics analysis, providing fast, accurate, reliable, and affordable sequencing services. We are able to offer our genomic sequencing services for samples from human, mouse, plant, animal and microbe. The mission of the CD Genomics is to facilitate genomics research by providing researchers access to cutting-edge technologies in the field of genomics. We are very flexible, and our services can be customized to fit your project needs, including customizable analysis specifically tailored to your needs. By consulting, we may have some suggestions on how we can help you to meet your specific research needs in the best and most economical way possible.

Our Genomics Solutions Include:

Whole Genome Sequencing

A comprehensive genome resequencing solution for samples from human and other species, with high coverage and great accuracy.

Whole Exome Sequencing

Powerful, efficient and cost-effective alternative to whole genome sequencing, with a focus on the exome enriched by commercial kits.

Targeted Region Sequencing

Obtain full DNA information of targeted regions or genes with greatly increased sequencing depths and reduced costs.

Viral Genome Sequencing

Create high-quality de novo assembly of novel viral genomes and help understand virus diversity, ecology, adaptation, and evolution.

Amplicon Sequencing

We offer an array of highly sensitive amplicon sequencing services like 16S/18S/ITS gene sequencing, CRISPR sequencing with fast turnaround times.

Chloroplast DNA (cpDNA) Sequencing

Chloroplast genome sequencing provides valuable insights into plant phylogeny and evolutionary adaption.

Complete Plasmid DNA Sequencing

Help us understand the genetic diversity and evolutionary history of plasmids, and the hot spots for the insertion of accessory genes.

Mitochondrial DNA (mtDNA) sequencing

A comprehensive and accurate tool for studies of human diseases, population genetics, and biodiversity assessments.

Long Amplicon Analysis (LAA)

Using Single Molecule, Real-Time (SMRT) Sequencing and the Sequel System produces highly accurate and phased CCSs from long amplicons.

* For Research Use Only. Not for use in diagnostic procedures.
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45-1 Ramsey Road, Shirley, NY 11967, USA
Tel: 1-631-275-3058 (USA)
       44-208-144-6005 (Europe)
Fax: 1-631-614-7828