CD Genomics-the genomics service company

CD Genomics

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Shotgun Sequencing Shotgun Sequencing

Providing profound metagenomics solution to fully sequence the majority of available genomes within a microbial community

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Whole Exome Sequencing Whole Exome Sequencing

Providing whole exome sequencing (WES) for both human and mouse

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PacBio SMRT Sequencing PacBio SMRT Sequencing

Providing long-reads sequencing to achieve full-length metagenomics and full-length transcripts study

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RNA Sequencing RNA Sequencing

Offering and tailoring transcriptomics services including mRNA-seq, small RNA sequencing, circRNA sequencing, lncRNA sequencing, and

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Epigenomics Sequencing Epigenomics Sequencing

Offering genome-wide epigenomics analysis to accommodate various sample types and suit your needs

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SNP Genotyping SNP Genotyping

Providing a fully flexible genotyping service including MassARRAY, KASP, SNaPshot, and Whole-genome SNP genotyping services

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Visit our Resource Center to learn more about our scientists' expertise through the scientific support documents we've developed, including sample submission guidelines, principles, applications, and bioinformatics of genetic technologies.

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CD Genomics to Present at BIO International Convention 2022 June 10, 2022

CD Genomics, a world-leading genomics services company, today announced that members of its management team will participate in the BIO International Convention...

Press release
Microbial Fingerprints, Health Insights Gleaned from Individual Gut Microbiome Dynamics April 9, 2021

NEW YORK – A new sequencing study suggests gut microbial communities are individualized and relatively stable over time, though the extent of that genetic stability varies somewhat with the microbial species considered. Researchers from the Netherlands and Israel did metagenomic sequencing on fecal samples from...

Press release
Low-Coverage Sequencing Effectively IDs Novel Variants in Underrepresented Populations March 26, 2021

NEW YORK – An international group of researchers has shown that low-coverage sequencing can effectively identify novel variants in the genomes of individuals from populations that are currently underrepresented in genomic databases, and can help overcome challenges presented by common genotyping arrays....

Press release
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