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 Whole Genome Sequencing Services.
Whole genome sequencing (WGS) provides the most comprehensive analysis of genome variance and structure. WGS enables accurate detection of SNV, and structural variation of human genomes, or de novo assembly and variant detection of non-human genomes.
Human WGS: accurate SNV detection using the Illumina NovaSeq platform with or without variant calls. For clinical samples we offer NATA-accredited workflow.
Small WGS: AGRF offers a sample preparation and sequencing options suitable for a single or hundreds of microbial genomes.
Low Pass WGS: accurately measure genome-wide variance in populations. Applications range from GWAS to trait-mapping and selection in agriculture.
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
