CD Genomics is the pioneer in genomics research. Our experts and technicians are knowledgeable and have years of experience providing Genome Analysis Services.
DNA or RNA from multiple sources may be analyzed including fresh-frozen tissues, formalin-fixed, paraffin-embedded (FFPE) tissues, laser-capture micro-dissected cells and cell lines.
Our team offers a full range of both short-read (Illumina) and long-read (Pacific Biosciences) next-generation sequencing, gene expression, genotyping and DNA methylation applications, including:
Library preparation for Illumina, PacBio and 10X single cell sequencing
Whole-genome sequencing
Whole-genome methylation
Whole transcriptome (RNA Seq)
Targeted sequencing (QiaSeq, Agilent)
Small RNA (microRNA)
Reduced representational bisulfite sequencing (RRBS)
Microarrays for genome-wide genotyping (Illumina Infinium)
Sample Identification Validation (SIDV)
10X Genomics single cell analyses
No-Amp CRISPR/Cas-9 Targeting (PacBio)
Iso-Seq (PacBio)
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 Genome Analysis Services.
For research use only, not intended for any clinical use.
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