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Chris Bellas 2020. Gapclosing metagenomic islands. protocols.io https://dx.doi.org/10.17504/protocols.io.bix8kfrwCopy Citation Copied
URL: https://dx.doi.org/DOI:10.17504/protocols.io.bix8kfrw
Authors: Chris Bellas
Summary: This protocol allows gapclosing of metagenomic islands which occur when mapping metagenomic reads to a phage reference genome. These gaps arise because multiple gene variants co-exist for specific points on the genome, these variants fluctuate in dominance over space and time. This means mapping metagenomic reads from one location onto a phage reference genome from another will often result in multiple metagenomic islands. These gaps can be closed with the following protocol, allowing the other gene variants present in a phage pan-genome to be detected. The protocol relies on detection of the same phages in similar ecosystems and relies on the phage being sequenced to sufficient depth in each sample to allow metagenomic assembly of large contigs (>10 X coverage). Prerequisites:Bowtie2Geneious software packageSPAdes assembler Blast+ tools
Associated Publications: Bellas CM, Schroeder DC, Edwards A, Barker G, Anesio AM, Flexible genes establish widespread bacteriophage pan-genomes in cryoconite hole ecosystems. Nature Communications doi: 10.1038/s41467-020-18236-8
Affiliations: University of Innsbruck
External URL: https://doi.org/10.1038/s41467-020-18236-8
Version: 1
Publication Date: 2020
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