2021-05-19 11:14
Targeted RNA-sequencing selects and sequences subset transcripts of interests, increasing the coverage of a focused set of RNA sequences. It is an accurate method that generates genomic and gene-expression information of specific genome regions. The
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2021-05-19 11:14
CD genomics combines proven ribosomal reduction library preparation chemistries and illumina NGS technology into a single, streamlined protocol. Ribo-Zero ribosomal RNA reduction chemistry minimizes ribosomal contamination and maximizes the percentag
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2021-05-19 11:14
CD Genomics provides viral genome sequencing service within Illumina and PacBio Platforms. We can create high-quality de novo assembly of large viral genomes and highest possible data quality at low cost.

2021-05-19 11:13
CD Genomics provides complete plasmid DNA sequencing service, and our improved bioinformatics pipelines are available to perform de novo assembly with no reference required.

2021-05-19 11:13
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 amplicon sequencing services to meet your project req
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2021-05-19 11:13
CD Genomics is providing PacBio Single Molecular Real-Time (SMRT) sequencing to increase your research method for bacterial whole genome sequencing. A comprehensive view of the bacterial genome, including genes, regulatory regions, IS elements, phage
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2021-05-19 11:12
CD Genomics provides a fast, one-stop bacterial RNA sequencing solution from the quality control of sample to comprehensive data analysis. Please contact us for more information and a detailed quote.

2021-05-19 11:12
CD Genomics provides statistical and bioinformatic data analysis services that help our customers to explain large amounts of data generated by sequencing, genotyping, and microarray experiments.

2021-04-22 21:34
We provide professional SMRT-based transcriptomics analysis service to identify novel transcript isoforms, fusion gene expression and alternative splicing events, and improve genome annotation.