Next Generation Sequencing

Next Generation Sequencing

As the demand for in-depth genetic research increases, traditional sequencing technologies are no longer able to meet the needs of researchers for in-depth genetic information. Next-generation sequencing (NGS) is widely recognized by researchers as a technology capable of massively parallel or deep sequencing of selected regions of an organism or the entire genome and has become one of the most commonly used techniques in biological and medical research.

As a world-class sequencing company, CD Genomics has built a cutting-edge next-generation sequencing technology platform. Based on the advanced sequencing platform, we provide customers with comprehensive and personalized sequencing services. Our NGS technology can sequence the entire genome or specific regions of DNA or RNA, helping researchers explore the relationship between genes and diseases, and genes and life activities.

Our Next Generation Sequencing Services

• Next-Generation RNA-Seq: Our next-generation RNA-sequencing projects including total RNA-seq, mRNA-seq, miRNA & small RNA-seq, lncRNA-seq, circRNA-seq, CAGE-seq, etc., can reveal gene expression profiles and describe the continuum in the transcriptome changes, helping to explore the underlying transcriptional and regulatory network mechanisms.
• Next-Generation DNA-Seq: Our next-generation DNA sequencing includes ChIP-seq, CUT&Tag seq, Hi-C seq, ATAC-seq, micro-C seq, amplicon sequencing, whole genome sequencing, whole exome sequencing, targeted sequencing, whole genome resequencing, metagenomic sequencing, microbiome Sequencing, TCR Beta sequencing, BCR sequencing, and other projects can simultaneously sequence and analyze hundreds of thousands to millions of DNA molecules to help researchers quickly obtain DNA information to explore how proteins interact with DNA, the relationship between diseases and genes, and more.
• Methyl-Seq: Our next-generation methylation sequencing, including projects such as whole genome bisulfite sequencing, and reduced representation bisulfite sequencing, enables the detection of methylation patterns in CpG, CHH, and CHG regions at the genome-wide level.
• Single Cell Sequencing: Our next-generation single-cell sequencing, including single-cell RNA sequencing, single-cell ATAC sequencing, single-nuclei RNA sequencing, and other projects, can examine the genome or transcriptome of a single cell, revealing heterogeneity differences between cells, providing information on cell-to-cell heterogeneity High-resolution view of variants.

Our Next Generation Sequencing Technology Platforms

• HiSeq X Ten
• NextSeq 500 NGS System
• Two MiSeq NGS Systems
• NovaSeq 6000 NGS System
• NextSeq 2000 NGS System
• 10× Genomics Chromium System, etc.

Applications

• HLA typing
• Basic genomics
• Agricultural genomics
• Genetic disease research
• Analysis of epigenetic factors
• Microbial diversity exploration
• Exploring the tumor microenvironment
• Identification and diagnosis of pathogens, etc.

Our Advantages

• NGS provides whole genome sequencing coverage while reducing sequencing costs.
• Capable of meeting the need for depth of information for today's complex genomic research problems.
• Capable of parallel, deep sequencing of hundreds of thousands to millions of nucleic acid molecules on a large number of samples simultaneously.

Our Workflow

CD Genomics' vision is to provide next-generation sequencing services to all researchers with sequencing needs. All of our services are handled by dedicated personnel, from sample preparation, library preparation, and sequencing to data analysis can be customized to meet your requirements. If you need NGS sequencing services, please feel free to contact us for assistance.

For research use only, not for any clinical use.