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Complete Genomics

From SNPedia


A company which provides human full genome sequencing. They've published their method.

Bought by the BGI in Sept 2012

In June 2011, User:David Ewing Duncan as part of the Personal Genome Project received data from Complete Genomics.

Promethease can read the dbSNPAnnotated.bz2 file, as well as the almost as useful masterVarBeta file.

These 37 samples are part of the reference data.

In Nov 2014 we saw some exome VCFs which came from Complete Genomics, but did not have an rs#s in teh 3rd column, so Promethease is unable to work with this data.