articleScienceNov 5, 2009Closed access

Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

Complete Genomics (United States) · Harvard University · +1 more institution

PubMed
Indexed incrossrefpubmed

Abstract

Genome sequencing of large numbers of individuals promises to advance the understanding, treatment, and prevention of human diseases, among other applications. We describe a genome sequencing platform that achieves efficient imaging and low reagent consumption with combinatorial probe anchor ligation chemistry to independently assay each base from patterned nanoarrays of self-assembling DNA nanoballs. We sequenced three human genomes with this platform, generating an average of 45- to 87-fold coverage per genome and identifying 3.2 to 4.5 million sequence variants per genome. Validation of one genome data set demonstrates a sequence accuracy of about 1 false variant per 100 kilobases. The high accuracy,…

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