2011
DOI: 10.1093/bioinformatics/btr216
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Meta-IDBA: a de Novo assembler for metagenomic data

Abstract: Motivation: Next-generation sequencing techniques allow us to generate reads from a microbial environment in order to analyze the microbial community. However, assembling of a set of mixed reads from different species to form contigs is a bottleneck of metagenomic research. Although there are many assemblers for assembling reads from a single genome, there are no assemblers for assembling reads in metagenomic data without reference genome sequences. Moreover, the performances of these assemblers on metagenomic… Show more

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Cited by 281 publications
(194 citation statements)
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References 23 publications
(40 reference statements)
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“…The MG-RAST quality control-passed reads were directly assembled using IDBA-ud (Peng et al, 2011) and only contigs longer than 200 bp were analyzed. Average coverage for each contig was calculated as the IDBA header designated read count multiplied by the average sequence length and divided by the length of the contig.…”
Section: Metagenome Assembly and Annotationmentioning
confidence: 99%
“…The MG-RAST quality control-passed reads were directly assembled using IDBA-ud (Peng et al, 2011) and only contigs longer than 200 bp were analyzed. Average coverage for each contig was calculated as the IDBA header designated read count multiplied by the average sequence length and divided by the length of the contig.…”
Section: Metagenome Assembly and Annotationmentioning
confidence: 99%
“…This exploits a convenient biological feature of metagenomic samples: They contain many microbes that should not assemble together. Graph partitioning has been used to improve the quality of metagenome and transcriptome assemblies by adapting assembly parameters to local coverage of the graph (23)(24)(25). However, to our knowledge, partitioning has not been applied to scaling metagenome assembly.…”
mentioning
confidence: 99%
“…The common k-mers were assembled using Minimo from the amos package (version 1.5; http://sourceforge.net/ projects/amos/ and Treangen et al, 2002) at 100% nucleotide identity and an overlap length of 50% and the adapter sequences were trimmed with Trimmomatic. Following trimming, DNA sequences were assembled using IDBA-UD (Peng et al, 2011(Peng et al, ,2012 using a k-mer range of 28-124 and default parameters.…”
Section: Sample Collection For Illumina Data Setsmentioning
confidence: 99%