Hi-C sequencing, as known as chromosome conformation capture sequencing, short for 3C-Seq, is a next-generation sequencing (NGS) based method for interpreting the interaction patterns among different DNA sequences, as well as providing high-resolution chromatin three-dimensional structure information. https://rna.cd-genomics.co...

RNA immunoprecipitation sequencing (RIP-seq) is a next-generation sequencing (NGS)-based method to comprehensively study the situation of intracellular RNA and its binding protein, a dynamic process of the post-transcriptional regulatory network. We provide a one-stop RIP-seq service to help customers discover new RNA-protein interaction sites and explore more gene regulation functions. https://rna.cd-genomics.co...

CD Genomics analyzes the microbes found in air, and their impact on human health using sequencing techniques like metagenomics sequencing, 16S/18S/ITS sequencing, and metranscriptomic sequencing. RT-qPCR is also used for achieving the qualitative and quantitative analysis of DNA or RNA. Bioinformatics analysis is required to process raw reads and determine the taxonomic classifications, biological functions for ecological environment, and effects on human health. https://www.cd-genomics.co...

The gut microbiota represents a thriving and intricate community of symbiotic microbes inhabiting the animal gastrointestinal tract. Comparable to an organ in its own right, gut microbiota conduct a plethora of physiological functions that encompass metabolism, immunological regulation, and endocrine operations. Beneficial microbes play a cardinal role in normal gut functionality: they aid in moisture absorption, vitamin synthesis, the mitigation of harmful substances, and the prevention of pathogenic invasion. In contrast, an excess of harmful microbes can lead to invasive pathogens, alterations in gut motility, production of detrimental substances, and poor waste excretion. CD Genomics proffers leading-edge, integrated research solutions for the study of gut microbiota, employing advanced metabolomics and high-throughput sequencing technologies. https://www.cd-genomics.co...

As a leading provider of NGS services and a partner of Illumina, CD Genomics offers a portfolio of solutions for metagenomics sequencing. 16S amplicon sequencing is characterized by cost-efficiency, high-speed and practicability to help you identify and investigate the microbial community. With over 10 years of experience, we can totally meet your project requirements and budgets in the exploration of microbial biodiversity. https://www.cd-genomics.co...

Genome assembly is one of the main purposes of sequencing. De novo genome assembly is a strategy for genome assembly, representing the genome assembly of a novel genome from scratch without the aid of reference genomic data. De novo genome assemblies assume no prior knowledge of the source DNA sequence length, layout or composition. https://www.cd-genomics.co...

CD Genomics is committed to offering advanced next generation sequencing (NGS) strategy to help researchers screening the phage display libraries in a high-throughput manner, enabling you to preserve the diversity of antibody libraries and quickly select the plurality of related antibodies as well as rare phages in a large population that can be recovered and tested for activity. Illumina deep-sequencing provides many advantages to phage display library screening, especially for the large sequence collection. https://www.cd-genomics.co...

A service provider for the whole exome data analysis, CD Genomics uses bioinformatics to deeply mine the genetic information in the coding region based on the whole exome sequencing data. Our unique skills in data analysis can meet customers' personalized data analysis needs and provide you with comprehensive data analysis results. https://bioinfo.cd-genomic...

A variant detection and analysis service provider, CD Genomics uses bioinformatics to help you explore the genetic variation and decipher the essence of life. Our unique skills in data analysis can meet customers' personalized data analysis needs and provide you with comprehensive data analysis. https://bioinfo.cd-genomic...

UMI small RNA sequencing (RNA-seq) is a unique molecular identifier (UMI)-based technology for accurate qualitative and quantitative analysis of multiple small RNAs in cells. PCR amplification bias can be removed by adding UMI into each cDNA segment, achieving accurate and unbiased quantification. UMI small RNA-seq can accurately identify SNP, quantify low-abundance transcripts, and reveal comprehensive transcriptome information. We provide UMI small RNA-seq to help you analyze microRNA (miRNA), small interfering RNA (siRNA), piwi-interacting RNA (piRNA) at one time. https://rna.cd-genomics.co...