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MetaQUAST: evaluation of metagenome assemblies
Open accessAbstract
Summary: During the past years we have witnessed the rapid development of new metagenome assembly methods. Although there are many benchmark utilities designed for single-genome assemblies, there is no well-recognized evaluation and comparison tool for metagenomic-specific analogues. In this article, we present MetaQUAST, a modification of QUAST, the state-of-the-art tool for genome assembly evaluation based on alignment of contigs to a reference. MetaQUAST addresses such metagenome datasets features as (i) unknown species content by detecting and downloading reference sequences, (ii) huge diversity by giving comprehensive reports for multiple genomes and (iii) presence of highly relative species by detecting chimeric contigs. We demonstrate MetaQUAST performance by comparing several leading assemblers on one simulated and two real datasets. Availability and implementation: http://bioinf.spbau.ru/metaquast. Contact: aleksey.gurevich@spbu.ru Supplementary information: Supplementary data are available at Bioinformatics online.
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“Whole genomes of organisms, in addition to strain tracking, can be extracted from the data, allowing for evolutionary analysis of specific organisms associated with a particular disease or environment.79, 80, 81”
From The oral microbiome: Role of key organisms and complex networks in oral health and disease (2021) · cites this paper as [79]
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Challenges and opportunities in sharing microbiome data and analyses
Huttenhower, C., Finn, R. D., & McHardy, A. C. (2023) · Nature Microbiology · doi:10.1038/s41564-023-01484-x · Cited by 74
“Benchmarking software, data and platforms AMBER 80 , OPAL 81 , CAMI platform 43 , LEMMI 82 , MetaQuast 83 , CAMISIM 84 , curatedMetagenomicData 58 Processed data figshare, Dryad, Zenodo, OSF, the Harvard Dataverse , PANGAEA, MGnify (MAGs) Few repositories allow pre-analysed microbiome data…”
MethodColman, D. R., Lindsay, M. R., & Boyd, E. S. (2019) · Nature Communications · doi:10.1038/s41467-019-08499-1 · Cited by 75
Ghimire, S., Roy, C., Wongkuna, S., Antony, L., Fenske, G. J., Maji, A., Keena, M. C., Foley, A., & Scaria, J. (2020) · mSystems · doi:10.1128/msystems.00620-19 · Cited by 71
Tutorial: assessing metagenomics software with the CAMI benchmarking toolkit
Meyer, F., Lesker, T.-R., Koslicki, D., Fritz, A., Gurevich, A. A., Darling, A. E., Sczyrba, A., Bremges, A., & McHardy, A. C. (2021) · Nature Protocols · doi:10.1038/s41596-020-00480-3 · Cited by 74
“Evaluation metrics are extensively tested and implemented in the MetaQUAST 23 , AMBER 24 , and OPAL 25 benchmarking packages (Table 3), available via Bioconda 26 .”
MethodSelf-citationBlawid, R., Silva, J. M. F., & Nagata, T. (2017) · Annals of Applied Biology · doi:10.1111/aab.12345 · Cited by 69
Bioinformatics tools to assess metagenomic data for applied microbiology
de Almeida, O. G. G., & Martinis, E. C. P. D. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-9464-9 · Cited by 68
Natural products from reconstructed bacterial genomes of the Middle and Upper Paleolithic
Klapper, M., Hübner, A., Ibrahim, A., Wasmuth, I., Borry, M., Haensch, V. G., Zhang, S., Al‐Jammal, W. K., Suma, H. R., Yates, J. A. F., et al. (2023) · Science · doi:10.1126/science.adf5300 · Cited by 67
Evaluating metagenomics and targeted approaches for diagnosis and surveillance of viruses
Buddle, S., Forrest, L., Akinsuyi, N., Bernal, L. M. M., Brooks, T., Venturini, C., Miller, C. M., Brown, J. R., Storey, N., Atkinson, L., et al. (2024) · Genome Medicine · doi:10.1186/s13073-024-01380-x · Cited by 70
“The assembly of the resulting contigs (> 150nt only) was assessed using metaQUAST [82].”
MethodLong-read metagenomics of soil communities reveals phylum-specific secondary metabolite dynamics
Goethem, M. W. V., Osborn, A. R., Bowen, B. P., Andeer, P. F., Swenson, T. L., Clum, A., Riley, R. W., He, G., Koriabine, M., Sandor, L., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02809-4 · Cited by 62
Accurate identification of bacteriophages from metagenomic data using Transformer
Shang, J., Tang, X., Guo, R., & Sun, Y. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbac258 · Cited by 63
The highly diverse Antarctic Peninsula soil microbiota as a source of novel resistance genes
Marcoleta, A. E., Arros, P., Varas, M. A., da Costa, J. R. N., Rojas-Salgado, J., Berríos-Pastén, C., Tapia-Fuentes, S., Silva, D., Fierro, J. F., Canales, N., et al. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.152003 · Cited by 61
MATAM: reconstruction of phylogenetic marker genes from short sequencing reads in metagenomes
Péricard, P., Dufresne, Y., Couderc, L., Blanquart, S., & Touzet, H. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btx644 · Cited by 60
Padilla, C. C., Bertagnolli, A. D., Bristow, L. A., Sarode, N., Glass, J. B., Thamdrup, B., & Stewart, F. J. (2017) · Frontiers in Marine Science · doi:10.3389/fmars.2017.00023 · Cited by 59
“The number of contigs, contig length, GC content, N50, and L50 assembly statistics were calculated with metaQUAST (Mikheenko et al., 2016; Supplementary Table 2).”
MethodGauge your phage: benchmarking of bacteriophage identification tools in metagenomic sequencing data
Ho, S. F. S., Wheeler, N. E., Millard, A. D., & van Schaik, W. (2023) · Microbiome · doi:10.1186/s40168-023-01533-x · Cited by 71
Bishara, A., Moss, E. L., Tkachenko, E., Kang, J. B., Zlitni, S., Culver, R. N., Andermann, T. M., Weng, Z., Wood-Bouwens, C. M., Handy, C., et al. (2020) · Genome Medicine · doi:10.1186/s13073-020-00747-0 · Cited by 53
Functional Strain Redundancy and Persistent Phage Infection in Swiss Hard Cheese Starter Cultures
Somerville, V., Berthoud, H., Schmidt, R. S., Bachmann, H.-P., Meng, Y. H., Fuchsmann, P., von Ah, U., & Engel, P. (2022) · The ISME Journal · doi:10.1038/s41396-021-01071-0 · Cited by 55
Mikheenko, A., Bzikadze, A. V., Gurevich, A. A., Miga, K. H., & Pevzner, P. A. (2020) · Bioinformatics · doi:10.1093/bioinformatics/btaa440 · Cited by 53
Self-citationMarasco, R., Fusi, M., Ramond, J., Goethem, M. W. V., Seferji, K. A., Maggs‐Kölling, G., Cowan, D. A., & Daffonchio, D. G. (2022) · ISME Communications · doi:10.1038/s43705-022-00130-7 · Cited by 57
“2 [66] after which we identified open reading (ORFs) using Prodigal v2.”
MethodAuxiliary Metabolic Gene Functions in Pelagic and Benthic Viruses of the Baltic Sea
Heyerhoff, B., Engelen, B., & Bunse, C. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.863620 · Cited by 55
Increasing the power of interpretation for soil metaproteomics data
Jouffret, V., Miotello, G., Culotta, K., Ayrault, S., Pible, O., & Armengaud, J. (2021) · Microbiome · doi:10.1186/s40168-021-01139-1 · Cited by 52
Męcik, M., Buta, M., Paukszto, Ł., Maździarz, M. A., Wolak, I., Harnisz, M., & Korzeniewska, E. (2023) · Journal of Environmental Management · doi:10.1016/j.jenvman.2023.119303 · Cited by 52
Pandolfo, M., Telatin, A., Lazzari, G., Adriaenssens, E. M., & Vitulo, N. (2022) · mSystems · doi:10.1128/msystems.00741-22 · Cited by 51
“Finally, the last part of the report provides general statistics about read quality check/preprocessing and assembly metrics (calculated using the metaQuast tool [18]).”
MethodNair, S., Zhang, Z., Li, H., Zhao, H., Shen, H., Kao, S., Jiao, N., & Zhang, Y. (2022) · Science Advances · doi:10.1126/sciadv.abf4792 · Cited by 51
De novo haplotype reconstruction in viral quasispecies using paired-end read guided path finding
Chen, J., Zhao, Y., & Sun, Y. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty202 · Cited by 50
Shi, B., Zhao, R., Su, G., Liu, B., Liu, W., Xu, J. F., Li, Q., & Meng, J. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.162031 · Cited by 51
Phables: from fragmented assemblies to high-quality bacteriophage genomes
Mallawaarachchi, V., Roach, M. J., Decewicz, P., Papudeshi, B. N., Giles, S. K., Grigson, S. R., Bouras, G. S., Hesse, R. D., Inglis, L. K., Hutton, A. L. K., et al. (2023) · Bioinformatics · doi:10.1093/bioinformatics/btad586 · Cited by 49
“We evaluated the resolved phage genomes using metaQUAST (Mikheenko et al. 2016).”
Meiser, A., Otte, J., Schmitt, I., & Grande, F. D. (2017) · Scientific Reports · doi:10.1038/s41598-017-14576-6 · Cited by 51
The Earth BioGenome project: opportunities and challenges for plant genomics and conservation
Expósito‐Alonso, M., Drost, H., Burbano, H. A., & Weigel, D. (2019) · The Plant Journal · doi:10.1111/tpj.14631 · Cited by 47
Metadata
- Authors
- Mikheenko, A., Saveliev, V., & Gurevich, A.
- Affiliations
- St Petersburg University (RU)
- Corresponding author
- Gurevich, Alexey
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2015-11-26
- Volume
- 32
- Issue
- 7
- Pages
- 1088-1090
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- OpenAlex
- W2175526948
- Cited by
- 711
- References
- 27
- Citations by year
- 2026: 76 · 2025: 100 · 2024: 104 · 2023: 92 · 2022: 78 · 2021: 82 · 2020: 57 · 2019: 44 · 2018: 34 · 2017: 34 · 2016: 9 · 2015: 1
- FWCI
- 11.30
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Bioinformatics (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Russian Science Foundation (14‐50‐00069, 14-50-)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Physical Sciences › Environmental Science › Ecology › Environmental DNA in Biodiversity Studies
- Life Sciences › Immunology and Microbiology › Virology › Bacteriophages and microbial interactions
- Keywords
- metagenome assembly, assembly evaluation, QUAST, assembler comparison, contig alignment
- MeSH terms
- Algorithms, Software, Metagenome, Metagenomics, Genomic Structural Variation
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