Complete Genomics, Inc. is a leading commercial provider of complete
human genome sequencing services.
Not exact matches
For the Standard
Sequencing Service, all of these variation types are identified in comparison to the
human genome reference.
Complete Genomics provides free public access to a variety of whole
human genome data sets generated from Complete Genomics»
sequencing service.
While these variants are all determined in comparison to the
human genome reference,
genomes submitted for the Cancer
Sequencing Service are additionally analyzed for somatic variants called in comparison to the baseline
genome within the submitted pair or trio.