Combining the continuous development and data explosion of modern NGS sequencing technology and its extensions, CD Genomics develops bioinformatics analysis pipelines based on NGS platforms to integrate multi-omics data from genomics, transcriptomics, microbiomics, and epigenomics, etc. to easily respond to various needs of academic and preclinical research. We are committed to transforming raw sequencing data into meaningful biological results.
The rapid development of next-generation sequencing (NGS) technology has led genomics into a new era. Although NGS technology has high throughput and can efficiently sequence multiple genes in parallel at ideal coverage depths, it is difficult for researchers to understand the significance of a large amount of data due to its limited sequencing read length and the large amount of data generated, which requires multiple tools for bioinformatics analysis such as sequence alignment and variant annotation. CDG has created a faster and more complete solution for sequencing data analysis.
We provide primary/secondary/tertiary sequencing data analysis, from evaluation of raw sequencing data, to alignment and gene expression analysis, to in-depth analysis and biological interpretation of genetic features for different needs, presented in visualization to support your project or downstream step design.
Our NGS data analysis services (but not limited to)
|Raw Data Assessment
|Data Distribution Analysis
|Dimensional Reduction & Clustering Analysis
|Differential Expression Analysis
|Structural Variant Analysis
|Gene Regulation Analysis
|Alternative Splicing Analysis
|Gene Ontology Enrichment Analysis
|Pathway Enrichment Analysis
|Protein-Protein Interaction Network
|Co-Expression Network Analysis
CD Genomics is developing comprehensive bioinformatics solutions using NGS and long-read sequencing data analysis to accelerate your scientific and pharmaceutical R&D breakthroughs and help you solve complex sequencing data analysis problems. Our dedicated team of experts performs quality management and follows every procedure, and has helped many customers get better and faster access to useful information to accelerate research in genomics, genetics, and other sciences and drug development.
We can handle many file types, including FASTQ, BED, SAM, BAM, VCF, etc.
Our goal is not only to act as a data analysis service provider, but also as a consultant for your project, providing a total service from project design, data generation, project advancement, data analysis and visualization reporting. If you have further needs, please contact us for more detailed information.