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Epigenomics Sequencing

We offer dozens of technologies to help you study the effects of epigenomic modifications that cause diseases and disorders in plants, animals and humans.

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SNP Genotyping

With our services you can either take a deep look into the genome and search for unknown genotype-phenotype connections or genotype already known variations.

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PacBio SMRT Sequencing

With longer reads, we can sequence through extended repetitive regions and detect mutations， sequence full-length transcripts or fragments with significant lengths and provide information on genome-wide DNA modification.

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Metagenomics Solution

We offer a suite of metagenomics solutions ranging from targeted assays (16S for prokaryotes and ITS2 for fungi) to whole genome analysis.

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Explore Areas of Interest

Rooted in extensive experience in DNA and RNA sequencing, a deep understanding of molecular biology, and a wealth of bioinformatics knowledge, CD Genomics has been working with the world's leaders in pharmaceutical and biotechnology. We are capable of assisting your projects in the following areas:

Microbial Genomics

Comprehensive solutions to fully sequence the majority of available genomes within a microbial community

Genomics Sequencing

Offer our genomic sequencing services for samples from human, mouse, plant, animal and microbe.

Epigenomics Sequencing

Provide comprehensive and reliable genome-wide information regarding DNA methylation.

RNA Sequencing

Provide and customize transcriptomics services, including mRNA-sequencing, small RNA sequencing, circRNA sequencing, lncRNA sequencing, etc.

TCR-Sequencing

Unprecedentedly high-resolution picture of the TCR repertoire provides great potential for revealing dynamic changes in clonal populations during antigen stimulation.

SNP Genotyping

Detect common and rare SNPs, CNVs and other genetic variations.

Bioinformatics Services

NGS data or long read data analysis and interpretation.

Advances Platform

See all platforms

CD Genomics has established NGS and long-read sequencing platforms designed to meet the most demanding yet critical needs of basic research and preclinical applications.

PacBio SMRT Sequencing

By taking advantage of the long-read and single molecular sequencing capability developed by PacBio, we are proud to offer advanced genome de novo assembly solutions and full-length gene/transcript sequencing strategy to suit your project needs.

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Nanopore Sequencing

Nanopore technology for sequencing biomolecules has wide applications in the life sciences, including identification of pathogens, food safety monitoring, genomic analysis, metagenomic environmental monitoring, and characterization of bacterial antibiotic resistance.

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Hot Services

mtDNA Sequencing

Whole Genome Sequencing

Whole Exome Sequencing

16S/18S/ITS Amplicon Sequencing

Microbial Whole Genome Sequencing

Metagenomic Shotgun Sequencing

Genotyping by Sequencing (GBS)

Ribosome Profiling (Ribo-seq)

CRISPR Screen Sequencing

HLA Typing

Let's Make Something Great

We look forward to working with you in drug development, disease research, agriculture, etc., and let's do it.

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How Can We Help You?

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Case Study

Check out the sequencing services we provide to researchers from around the world to advance their discoveries and to power and energize.

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Sample Submission Guidelines

We strive to make the sample submission process as simple and efficient as possible to ensure the highest quality sequencing results for our customers.

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