We provide bioinformatics services to biomedical researchers in academic institutions, biotechnology and pharmaceutical industries, clinical institutions and government agencies. In addvition to providing advice and assistance in designing and implementing onerous bioinformatics research projects, our bioinformatics team also carries out heavy bioinformatics projects and research projects directly for our clients. We serve researchers and in diverse areas involving a wide range of organisms -from medical research using human samples or studies involving human patients, to animal and plant research using model or non-model organisms, to research projects targeting microbial and viral species.
We are engaged in many types of bioinformatics work, including but not limited to: processing, analyzing and interpreting high-throughput biological and medical data-focusing on next-generation sequencing (NGS) data, genomics, transcriptome, proteomics, microorganisms, epigenetics, metabolomics, and other combinatorial data, statistical data analysis, data integration for multiple biomedical and other data types - e.g., used to identify causality or other hidden information between measurement variables, statistical models, development and application of machine learning methods, macrogenomics, ecology, phylogeny, population genetics and other analysis related to evolutionary biology, data mining, customization and advanced analytical method development, specific data structures and algorithm development, informatics, database development and maintenance, software solutions as well as IT and infrastructure solutions.
Our team is experienced in processing NGS data from all common platforms, including Illumina, Ion Torrent, 454, Solid, PacBio and Oxford Nanopore. And all common NGS applications-including whole genome sequencing (map-based or assembly-based applications), exome and other targeted sequencing, RNA-SEQ, CHIP-SEQ (for transcription factor, RNA PolII and histone modification), and various sequencing-based DNA methylation applications. We are also experienced in less commonly used NGS applications, such as Hi-C Seq, QTL-Seq, RRBS, ATAC-Seq, MeRIP-seq and RIP-seq. In addition, we also have the ability to assist in the development of new NGS applications. We have extensive experience in processing microarray data from all major array platforms (Affymetrix, Agilent, Illumina and NimbleGen) for a variety of applications, including gene expression profile analysis, DNA methylation analysis, genotyping, etc.
Data analysis includes upload raw data, quality control (QC), statistical analysis,
chart production and result reporting. Analysis contents include differential expression analysis of genes, functional enrichment analysis, signal pathway enrichment analysis, interaction network analysis,
pathway enrichment analysis, and various cluster analysis.
In this process, Linux, Perl, Python, R and other languages and biological information analysis software are used for data analysis and chart making.
Provide safe and reliable storage services for the entire data life cycle
Save your precious time and speed up the research process
Make your data simple and clear, directly used in the next research
Since the first high-throughput sequencer was put on the market in 2005, the cost of sequencing
has been greatly reduced with the continuous innovation of gene sequencing technology in the past ten years.
With the decline in the cost of sequencing, major research institutions around the world have increased their investment in the field of genetic research, so genetic data are accumulating at a rate beyond Moore's law.
According to incomplete statistics, the world has accumulated more than billions of petabytes of genetic data.
Therefore, how to make good use of these data resources and mine the potential scientific research value of data through bioinformatics methods in the era of gene big data has become an important issue
in the new era of life science.
Our platform brings together a large number of high-level bioinformatics analysis talents from famous universities and scientific research institutes around the world, who have many years of practical experience in the field of bioinformatics research and development.
CD Genomics provides fast turnover and high-quality service to customers
all over the world at competitive prices. Our customers can contact our employees directly and respond to their inquiries in a timely manner. If you are interested in our service,
please contact us for more details.