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 Clinical Genomics Services.
Targeted short-read sequencing
RNA analysis
Ultrasensitive variant detection
Array-based SNP analysis
Bioinformatics support
Clinical interpretation of variants
2 x NextSeq 550 (Illumina)
MiSeq (Illumina)
Instrument for microarray analysis (Illumina)
MinION (Oxford Nanopore)
Digital droplet PCR (BioRad)
Real time PCR (BioRad)
QuantStudio 6 Flex Real-Time PCR (ThermoScientific)
Multispectral imaging microscope
Instrumentation for Sanger sequencing
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
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