Next-generation sequencing has fundamentally revolutionized biological and medical sciences. A sequencing/microarray data analysis project requires careful planning, seasoned methodology, and concise reporting. CD genomics is an expert company offering comprehensive bioinformatics solutions in all aspects of sequencing and microarray. We provide data analysis services for data generated by a wide range of sequencing/microarray platforms. We use the cutting-edge bioinformatics algorithms and pipeline, and provide you with high-quality and ready-for-publication figures. Our bioinformatic staff consists of PhD-level scientists trained in computer languages, statistics, bioinformatics, genetics, and genomics. The software infrastructure for analysis is a combination of custom-built and open-source software. Our bioinformatics services take your raw next/third generation data and provide you with comprehensive figures customized to your research purposes as well as personalized data interpretation support. CD Genomics’ full range of bioinformatics services can be an ideal solution for you.

High-throughput sequencing technology can generate numerous data with heterogeneous quality, and there is no optimal bioinformatics pipeline for all cases. We are specialized in customizing the bioinformatics pipeline for your specific projects. We support companies and research groups by turning ideas into concrete project plans and implementing them, thereby making full use of your data.

• Custom bioinformatics

• Illumina, Ion Torrent, PacBio SMRT, and Nanopore compatible

• Publication-ready data and figures

• Accurate sequencing and microarray services available

• A professional and experienced expert team

• Fast turnaround time

We aim to provide the highest level of service, confidentiality and customer support. Our extensive expertise can help expedite your SNP and mutation analysis assays with speed, quality, and reliability. With our services you can either take a deep look into the genome or search for unknown genotype-phenotype connections or genotype already known variations.