CD Genomics is the pioneer in genomics research. Our experts and technicians are knowledgeable and have years of experience providing Sanger Sequencing Services.
Our team offers a wide range of services utilizing the Illumina Novaseq 6000, NextSeq and Miseq. We have extensive knowledge of DNA/RNA library preparation and capture protocols.
Our platforms utilize PCR, proprietary BigDye 3.1 chemistry and capillary electrophoresis to provide high quality sequence reads for specific targets. Fragment analysis of insertion/deletions and microsatellite repeats also available.
Sequence PCR products, plasmids, BACs, etc.
Fast turnaround times and “machine-only” service available
Primer design and primer optimization services
Industry leading NGS validation
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 Sanger Sequencing Services.
For research use only, not intended for any clinical use.
Online Inquiry
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