BUSCO Update: Novel and Streamlined Workflows along with Broader and Deeper Phylogenetic Coverage for Scoring of Eukaryotic, Prokaryotic, and Viral Genomes
By Mosè Manni, Matthew Berkeley, Mathieu Seppey, Felipe A. Simão, E. Zdobnov. Molecular biology and evolution, 2021
5,249 citations recorded by the source corpus.
Abstract Methods for evaluating the quality of genomic and metagenomic data are essential to aid genome assembly procedures and to correctly interpret the results of subsequent analyses. BUSCO estimates the completeness and redundancy of processed genomic data based on universal single-copy orthologs. Here, we present new functionalities and major improvements of the BUSCO software, as well as the renewal and expansion of the underlying data sets in sync with the OrthoDB v10 release. Among the major novelties, BUSCO now enables phylogenetic placement of the input sequence to automatically select the most appropriate BUSCO data set for the assessment, allowing the analysis of metagenome-assembled genomes of unknown origin. A newly introduced genome workflow increases the efficiency and runtimes especially on large eukaryotic genomes. BUSCO is the only tool capable of assessing both eukaryotic and prokaryotic species, and can be applied to various data types, from genome assemblies and metagenomic bins, to transcriptomes and gene sets.
Subfields: Ecology, Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/d7216a4c00b0f525c7e57e433d8fe0b91db9ff53
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Citations in the corpus
- UniProt: the Universal Protein Knowledgebase in 2025 (2024, positive): “We continue to assess the quality of the remaining proteomes, using BUSCO ( 8 ) and the complete proteome detector ( 9 ).”
- Identification of mobile genetic elements with geNomad (2023, positive): “Lastly, 741 markers for universal single-copy genes, which are rarely present in MGEs and can help reduce false positives, were identified through comparison with profiles from the BUSCO dataset 25 .”