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Nat Biotechnol. 2012 Jul 1;30(7):693-700. doi: 10.1038/nbt.2280.

Hybrid error correction and de novo assembly of single-molecule sequencing reads.

Author information

1
National Biodefense Analysis and Countermeasures Center, Frederick, Maryland, USA. korens@nbacc.net

Abstract

Single-molecule sequencing instruments can generate multikilobase sequences with the potential to greatly improve genome and transcriptome assembly. However, the error rates of single-molecule reads are high, which has limited their use thus far to resequencing bacteria. To address this limitation, we introduce a correction algorithm and assembly strategy that uses short, high-fidelity sequences to correct the error in single-molecule sequences. We demonstrate the utility of this approach on reads generated by a PacBio RS instrument from phage, prokaryotic and eukaryotic whole genomes, including the previously unsequenced genome of the parrot Melopsittacus undulatus, as well as for RNA-Seq reads of the corn (Zea mays) transcriptome. Our long-read correction achieves >99.9% base-call accuracy, leading to substantially better assemblies than current sequencing strategies: in the best example, the median contig size was quintupled relative to high-coverage, second-generation assemblies. Greater gains are predicted if read lengths continue to increase, including the prospect of single-contig bacterial chromosome assembly.

PMID:
22750884
PMCID:
PMC3707490
DOI:
10.1038/nbt.2280
[Indexed for MEDLINE]
Free PMC Article
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