Genomicsness

Viral genome sequencing

CD genomics platform holds great potential for viral genome sequencing. A comprehensive virus sequences will facilitate interpretation of viral metagenomics data by providing reference genomes, lead to a better understanding of virus diversity, ecology, adaptation and evolution, and enable the prediction of emerging infectious diseases caused by viruses.

Targeted amplicon sequencing

 Whether you would like to detect the diversity of microbial communities or discover rare somatic mutations in complex samples. CD Genomics could provide professional, cost-efficient and high-speed targeted amplicon sequencing services to meet your project requirements.

single cell rna seq

Single-cell RNA Sequencing Workflow
The advent of cell sorting/partitioning technologies, such as flow cytometry and microfluidics, has made it possible to capture single cells, and the DNA or RNA of single cells is amplified for single-cell sequencing. 

Single cell rna

Gene expression research at the single-cell RNA resolution on samples composed of mixed cell populations allows for deep insight into c into the transcriptome complexity of diverse cell types.

bioinformatics companies

Our bioinformatic staff consists of all PhD-level scientists trained in bioinformatics companies.

Snp array

The Introduction to SNP array
Powered by state-of-the-art variant detection and SNP genotyping technologies, CD genomics provides the various of genotyping services, delivering high-quality data at a low per-sample cost.

Bioinformatic analysis

CD Genomics provides statistical and bioinformatic analysis services that help explain the large amounts of data.

Mitochondrial dna

Mitochondrial DNA sequencing is available on both Illumina’s MiSeq, and PacBio Sequel System.

Plasmid dna

Plasmid DNA sequencing is rapidly becoming a standard approach to increase our understanding of the genetic diversity and evolutionary history of plasmids. 

Bacterial rna

Bacterial RNA-Seq workflow’s first step is selection of mRNA transcripts.