Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays
Complete Genomics (United States) · Harvard University · +1 more institution
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,…
Citation impact
- FWCI
- 40.10
- Percentile
- 100%
- References
- 32
Authors
65- RDRadoje DrmanacCorresponding
Complete Genomics (United States)
- ABAndrew B. SparksCorresponding
Complete Genomics (United States)
- MJMatthew J. CallowCorresponding
Complete Genomics (United States)
- ALAaron L. HalpernCorresponding
Complete Genomics (United States)
- NBNorman BurnsCorresponding
Complete Genomics (United States)
Topics & keywords
- Human genome
- DNA
- Genome
- DNA sequencing
- Base (topology)
- Computational biology
- Base pair
- Biology