4.6 Article

Struo2: efficient metagenome profiling database construction for ever-expanding microbial genome datasets

期刊

PEERJ
卷 9, 期 -, 页码 -

出版社

PEERJ INC
DOI: 10.7717/peerj.12198

关键词

Metagenome; Database; Profiling; GTDB

资金

  1. Max Planck Society

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Mapping metagenome reads to reference databases is a standard approach for assessing microbial taxonomic and functional diversity. However, public reference databases often lack recently generated genomic data, limiting the sensitivity of readmapping. In order to address this issue and improve database comprehensiveness, the authors developed a faster database generation method, Struo2, along with custom databases that can be easily updated with new genomic content.
Mapping metagenome reads to reference databases is the standard approach for assessing microbial taxonomic and functional diversity from metagenomic data. However, public reference databases often lack recently generated genomic data such as metagenome-assembled genomes (MAGs), which can limit the sensitivity of readmapping approaches. We previously developed the Struo pipeline in order to provide a straight-forward method for constructing custom databases; however, the pipeline does not scale well enough to cope with the ever-increasing number of publicly available microbial genomes. Moreover, the pipeline does not allow for efficient database updating as new data are generated. To address these issues, we developed Struo2, which is >3.5 fold faster than Struo at database generation and can also efficiently update existing databases. We also provide custom Kraken2, Bracken, and HUMAnN3 databases that can be easily updated with new genomes and/or individual gene sequences. Efficient database updating, coupled with our pre-generated databases, enables assembly-enhancedprofiling, which increases database comprehensiveness via inclusion of native genomic content. Inclusion of newly generated genomic content can greatly increase database comprehensiveness, especially for understudied biomes, which will enable more accurate assessments of microbiome diversity.

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