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 Pacbio Sequencing Services.
We offer complete Pacbio library prep, BluePippin size selection and sequencing services. The base calling and secondary analyses like Reads-Of-Insert extraction, HGAP assembly, and IsoSeq analyses of single or a small number of SMRT-cells are included in the service.
Samples can be provided as already isolated DNA by the customers. We do offer HMW-DNA isolation services for PacBio 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.
For research use only, not intended for any clinical use.
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