SprayNPray: user-friendly taxonomic profiling of genome and metagenome contigs

BMC Genomics

Arkadiy I. Garber¹  Catherine R. Armbruster²  Vaughn S. Cooper²  Jennifer M. Bomberger²  Stella E. Lee³  Sean M. McAllister⁴ 

[1] Biodesign Center for Mechanisms of Evolution, Arizona State University;Department of Microbiology and Molecular Genetics, School of Medicine, University of Pittsburgh;Department of Otolaryngology, University of Pittsburgh Medical Center;Pacific Marine Environmental Laboratory, National Oceanic and Atmospheric Administration;

关键词: Symbiont;    Taxonomic classification;    Binning;    Bioinformatics;    Contaminant identification;    HGT;   

DOI  :  10.1186/s12864-022-08382-2

来源: DOAJ

【 摘 要 】

Abstract Background Shotgun sequencing of cultured microbial isolates/individual eukaryotes (whole-genome sequencing) and microbial communities (metagenomics) has become commonplace in biology. Very often, sequenced samples encompass organisms spanning multiple domains of life, necessitating increasingly elaborate software for accurate taxonomic classification of assembled sequences. Results While many software tools for taxonomic classification exist, SprayNPray offers a quick and user-friendly, semi-automated approach, allowing users to separate contigs by taxonomy (and other metrics) of interest. Easy installation, usage, and intuitive output, which is amenable to visual inspection and/or further computational parsing, will reduce barriers for biologists beginning to analyze genomes and metagenomes. This approach can be used for broad-level overviews, preliminary analyses, or as a supplement to other taxonomic classification or binning software. SprayNPray profiles contigs using multiple metrics, including closest homologs from a user-specified reference database, gene density, read coverage, GC content, tetranucleotide frequency, and codon-usage bias. Conclusions The output from this software is designed to allow users to spot-check metagenome-assembled genomes, identify, and remove contigs from putative contaminants in isolate assemblies, identify bacteria in eukaryotic assemblies (and vice-versa), and identify possible horizontal gene transfer events.

【 授权许可】

Unknown