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Complete Genomics publishes in Science on low-cost sequencing of 3 human genomes
Date:11/8/2009

e variants per genome processed.

Detailed validation of one genome dataset demonstrates a sequence accuracy of just one false variant per 100 kilobases, a remarkably low error rate, particularly for such an affordable technology.

Patterned genomic DNA nanoarrays and 70-base, unchained sequence reads are unique technical achievements. The company's new patterned genomic DNA nanoarrays, which achieve a record high density of 2.85 billion spots per slide at 0.7 micron pitch, will enable Complete Genomics to sequence 10,000 human genomes in 2010.


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Contact: Andrea Long
andreal@waggeneredstrom.com
503-702-8578
Complete Genomics
Source:Eurekalert  

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Complete Genomics publishes in Science on low-cost sequencing of 3 human genomes
Complete Genomics publishes in Science on low-cost sequencing of 3 human genomes
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