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Cited by 668

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

MetaVelvet: an extension of Velvet assembler to de novo metagenome assembly from short sequence reads

Open access
Namiki, Toshiaki, Hachiya, Tsuyoshi, Tanaka, Hideaki, Sakakibara, Yasubumi·2012·Nucleic Acids Research

Abstract

An important step in 'metagenomics' analysis is the assembly of multiple genomes from mixed sequence reads of multiple species in a microbial community. Most conventional pipelines use a single-genome assembler with carefully optimized parameters. A limitation of a single-genome assembler for de novo metagenome assembly is that sequences of highly abundant species are likely misidentified as repeats in a single genome, resulting in a number of small fragmented scaffolds. We extended a single-genome assembler for short reads, known as 'Velvet', to metagenome assembly, which we called 'MetaVelvet', for mixed short reads of multiple species. Our fundamental concept was to first decompose a de Bruijn graph constructed from mixed short reads into individual sub-graphs, and second, to build scaffolds based on each decomposed de Bruijn sub-graph as an isolate species genome. We made use of two features, the coverage (abundance) difference and graph connectivity, for the decomposition of the de Bruijn graph. For simulated datasets, MetaVelvet succeeded in generating significantly higher N50 scores than any single-genome assemblers. MetaVelvet also reconstructed relatively low-coverage genome sequences as scaffolds. On real datasets of human gut microbial read data, MetaVelvet produced longer scaffolds and increased the number of predicted genes.

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Metadata

Authors
Namiki, T., Hachiya, T., Tanaka, H., & Sakakibara, Y.
Venue
Nucleic Acids Research
Published
2012-07-19
Volume
40
Issue
20
Pages
e155-e155
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2109848222
Cited by
668
References
3
FWCI
23.47
Type
journal article
Language
en
Open access
gold

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