WELCOME TO CD GENOMICS
Genomics-Related Laboratory Services
CD Genomics offers various solutions, from genome-wide association studies on tens of thousands of samples to single SNP interrogations of several hundred individuals. Our experts and technicians are knowledgeable and have years of experience providing Bioinformatics Services.
Metagenomics analysis
Genome and transcriptome assembly and annotation
CRISPR target checking
Methylation (arrays, targeted and whole-genome bisulfite sequencing, PacBio long read sequencing)
Structural variant calling of whole genome sequencing data
Population genetics
Multilocus sequence typing (MLST)
ChIP-Seq
Cancer studies: SNP, Indel and CNV detection, tumour purity, structural variant detection
All of our custom contracts receive thorough data exploration and quality control. Our experienced bioinformaticians will supply a tailored analysis to meet your project goals. Data are summarised to the most important features and documented in a detailed and reproducible report.
CD Genomics has already updated its technology platforms to mainstream NGS, long-read sequencing, and microarray instruments. We continue to strive to offer the same reliable services to pharmaceutical and biotechnology companies, as well as academia and government agencies, for all your sequencing or array needs. If you are interested, please contact us directly for assistance.
For research use only, not intended for any clinical use.
Online Inquiry
Please fill out the form below and we will get back to you as soon as possible with a quotation for the item you are interested in.
SUITE 115, 17 Ramsey Road, Shirley, NY 11967, USA
Email: info@cd-genomics.org
Tel: 1-631-338-8059
Fax: 1-631-614-7828
