Evaluation of ddRADseq for reduced representation metagenome sequencing

Profiling of microbial communities via metagenomic shotgun sequencing has enabled researches to gain unprecedented insight into microbial community structure and the functional roles of community members. This study describes a method and basic analysis for a metagenomic adaptation of the double dig...

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Veröffentlicht in:PeerJ (San Francisco, CA) CA), 2017-09, Vol.5, p.e3837-e3837, Article e3837
Hauptverfasser: Liu, Michael Y, Worden, Paul, Monahan, Leigh G, DeMaere, Matthew Z, Burke, Catherine M, Djordjevic, Steven P, Charles, Ian G, Darling, Aaron E
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Sprache:eng
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Zusammenfassung:Profiling of microbial communities via metagenomic shotgun sequencing has enabled researches to gain unprecedented insight into microbial community structure and the functional roles of community members. This study describes a method and basic analysis for a metagenomic adaptation of the double digest restriction site associated DNA sequencing (ddRADseq) protocol for reduced representation metagenome profiling. This technique takes advantage of the sequence specificity of restriction endonucleases to construct an Illumina-compatible sequencing library containing DNA fragments that are between a pair of restriction sites located within close proximity. This results in a reduced sequencing library with coverage breadth that can be tuned by size selection. We assessed the performance of the metagenomic ddRADseq approach by applying the full method to human stool samples and generating sequence data. The ddRADseq data yields a similar estimate of community taxonomic profile as obtained from shotgun metagenome sequencing of the same human stool samples. No obvious bias with respect to genomic G + C content and the estimated relative species abundance was detected. Although ddRADseq does introduce some bias in taxonomic representation, the bias is likely to be small relative to DNA extraction bias. ddRADseq appears feasible and could have value as a tool for metagenome-wide association studies.
ISSN:2167-8359
2167-8359
DOI:10.7717/peerj.3837