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 Exome Sequencing Services.
Whole exome sequencing (WES) is a powerful tool for investigation of genetic variance across the protein coding regions of the genome. WES provides high coverage and high confidence in germline variant calls for the study of rare mendelian disorders, complex disease and cancer. AGRF provides comprehensive solutions for WES, including bioinformatics using gold standard tools (BWA and GTAK).
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.
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