Complete Genomics Ends Year with up to $9M in Revenue, 1,000 Genomes Order Backlog

This year, Complete Genomics plans to introduce a "long fragment read" technology that will allow it decrease the error rate from 10-5 to 10-7, or from 30,000 to 300 errors per genome, and to sequence genomes from fewer than 50 cells' worth of DNA.

Full-text access for premium subscribers only. Existing premium subscribers login here.
New to GenomeWeb? Register here quickly.