MetaSort untangles metagenome assembly by reducing microbial community complexity.
MetaSort untangles metagenome assembly by reducing microbial community complexity.
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MetaSort 通过降低微生物群落复杂性来理清宏基因组组装
DOI:
10.1038/ncomms14306
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发表时间:
2017-01-23
影响因子:
16.6
通讯作者:
Zhao F
中科院分区:
文献类型:
--
作者:
Ji P;Zhang Y;Wang J;Zhao F
Most current approaches to analyse metagenomic data rely on reference genomes. Novel microbial communities extend far beyond the coverage of reference databases and de novo metagenome assembly from complex microbial communities remains a great challenge. Here we present a novel experimental and bioinformatic framework, metaSort, for effective construction of bacterial genomes from metagenomic samples. MetaSort provides a sorted mini-metagenome approach based on flow cytometry and single-cell sequencing methodologies, and employs new computational algorithms to efficiently recover high-quality genomes from the sorted mini-metagenome by the complementary of the original metagenome. Through extensive evaluations, we demonstrated that metaSort has an excellent and unbiased performance on genome recovery and assembly. Furthermore, we applied metaSort to an unexplored microflora colonized on the surface of marine kelp and successfully recovered 75 high-quality genomes at one time. This approach will greatly improve access to microbial genomes from complex or novel communities. Currently available metagenomic data analysis relies on reference genomes. Here, the authors describe a new de novo metagenomic assembly method, metaSort, that constructs bacterial genomes from metagenomic samples to reduce microbial community complexity while increasing genome recovery and assembly.