CD genomics provides access to the genomic and genetic analysis at single cell level using 10x genomics system and its engineered reagent delivery method. The droplet-based platforms Chromium 10x System, powered by GemCode Technology, enables the biomedical researchers and clinicians to make important new discoveries using this powerful approach as the technologies and tools needed for conducting single cell studies. 10X genomics also permits to study cellular states in scenarios such as embryonal development, cancer, myoblast and lung epithelium differentiation, and lymphocyte fate diversification.

CD Genomics proprietary GenSeqTM Technology provides comprehensive Single-Cell Sequencing services. These global gene expression patterns in single cells already have dramatically advanced cell biology.

CD Genomics provides robust transcriptome research service down to single-cell input levels in high-quality samples These global gene expression patterns in single cells already have dramatically advanced cell biology.

CD Genomics has extensive experience in offering Iso-Seq service by producing full-length transcripts without assembly. Strict quality control following every procedure is executed to ensure the comprehensive and accurate results.

CD Genomics provides fungal whole genome sequencing with the PacBio Sequel system to offer more insights into genetic structure and functions. We are best in the knowledge, practise, and experience.

Creative proteomics provides high quality western blot service

Creative Proteomics Provides Hige Quality Western Blot Service.

Creative Proteomics provides N-terminal sequence analysis by both Edman and Mass spectrometry of therapeutic proteins, monoclonal antibodies and protein vaccines.

Creative Proteomics provides N-terminal sequence analysis by both Edman and Mass spectrometry of therapeutic proteins, monoclonal antibodies and protein vaccines.

DNA methylation is recognized as a principal contributor to the normal development and regulation of gene expression. It is essential for maintenance of cellular identity and is associated with a number of key processes including genomic imprinting, X-chromosome inactivation, repression of transposable elements, aging and carcinogenesis. The current method to research DNA methylation is only bulk. We combine the highly innovative single cell whole genome bisulfite sequencing (WGBS) library preparation and Illumina next-generation sequencing technology to visualize genomic methylation states at single-cell resolution. It single cell whole genome bisulfite sequencing enables the discovery of cellular heterogeneity typically masked by standard, bulk methylation sequencing. We provide a streamlined workflow for making WGBS libraries. Input DNA is randomly fragmented during the initial bisulfite treatment step followed by WGBS library preparation. The procedure can accommodate ultra-low DNA input making it ideal for methylation analysis of precious, limited, and target-enriched samples.CD Genomics provides single-cell DNA methylation analysis to understand the heterogeneity of genome-wide 5-methylcytosine (5mC) patterns.