CD Genomics is the pioneer in genomics research. Our experts and technicians are knowledgeable and have years of experience providing Whole Genome Genotyping and Copy Number Analysis Services.
To meet the sequencing needs of your project, sample preparation is fully automated on our workstations and tracked via the Genologics LIMS, enabling low-cost, high-quality data with competitive turnaround times and one-on-one customer service.
Whole genome genotyping arrays are an important tool for discovering variants that contribute to human disease. The two primary applications of this technology, genome-wide association studies (GWAS) and copy number variant (CNV) analysis unravel the complex genetic architecture of genetic traits and complex disease.
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 Genotyping and Copy Number Analysis Services.
For research use only, not intended for any clinical use.
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