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 direct RNA sequencing Services.
Direct RNA sequencing: this protocol is being implemented. The library preparation adds an adapter via annealing to the poly-A tail. The sequencing data can be used to investigate RNA-base modifications
The average sequence data yields can vary widely and will mostly depend on the sample properties (please see below). Average yields will be inversely correlated to the library molecule lengths (insert sizes). We have achieved the best run metrics mentioned below with DNA isolated from human/mammalian cell cultures and mammalian blood samples.
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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