MGnify: the microbiome analysis resource in 2020
Open accessAbstract
MGnify (http://www.ebi.ac.uk/metagenomics) provides a free to use platform for the assembly, analysis and archiving of microbiome data derived from sequencing microbial populations that are present in particular environments. Over the past 2 years, MGnify (formerly EBI Metagenomics) has more than doubled the number of publicly available analysed datasets held within the resource. Recently, an updated approach to data analysis has been unveiled (version 5.0), replacing the previous single pipeline with multiple analysis pipelines that are tailored according to the input data, and that are formally described using the Common Workflow Language, enabling greater provenance, reusability, and reproducibility. MGnify's new analysis pipelines offer additional approaches for taxonomic assertions based on ribosomal internal transcribed spacer regions (ITS1/2) and expanded protein functional annotations. Biochemical pathways and systems predictions have also been added for assembled contigs. MGnify's growing focus on the assembly of metagenomic data has also seen the number of datasets it has assembled and analysed increase six-fold. The non-redundant protein database constructed from the proteins encoded by these assemblies now exceeds 1 billion sequences. Meanwhile, a newly developed contig viewer provides fine-grained visualisation of the assembled contigs and their enriched annotations.
AI snapshot
Written from the paper’s full text.
TL;DR
MGnify’s 2020 update reports major growth of its microbiome analysis resource and the release of version 5.0, which replaces a single pipeline with multiple data-type-specific pipelines formally described in Common Workflow Language. It adds ITS-based taxonomy, expanded functional annotations, assembly-derived pathway/system predictions, a contig viewer, and a greatly expanded non-redundant protein database.
Key findings
- MGnify contains over 3,500 publicly available projects, comprising ∼175,000 samples, ∼230,000 runs and ∼240,000 analyses, a 2-fold increase in analysed datasets over two years; most analyses are 16S/18S rRNA amplicon (∼193,000), followed by metagenomic (∼27,000), assembly (∼16,000), metatranscriptomic (∼2,000) and metabarcoding (∼2,000).
- Pipeline v5.0, released September 2019, adds ITS1/2 taxonomic classification, KEGG orthologue predictions for reads and assembled contigs, and KEGG pathway and Genome Properties annotations for assembled contigs.
- MGnify has assembled ∼43,000 sequencing runs, mostly with metaSPAdes (<0.1% not due to memory limits), with about one third uploaded and analysed; the MGnify protein database grew from 50 million sequences (v2017_08) to over 1.1 billion (v2019_05), with only 9 million identical sequences shared with UniProtKB.
- A new contig viewer uses the Integrative Genomics Viewer framework, and “Super Studies” group related projects, such as all 96 Earth Microbiome Project studies and 8 Tara Oceans datasets.
Methods
- This is a resource-update paper describing MGnify’s data model, accessions (MGYS, MGYA, MGYP), ENA/INSDC integration, and analysis of user-submitted and public microbiome datasets.
- Version 5.0 uses separate CWL-described pipelines for amplicon, metagenomic/metatranscriptomic raw reads, and assemblies, executed with toil-cwl-runner; tools include SeqPrep, Trimmomatic, Rfam, MAPseq with SILVA/ITSoneDB/UNITE, mOTUs2, FragGeneScan, InterPro, Pfam, KEGG/KOfam, Prodigal, eggNOG-mapper, antiSMASH, and DIAMOND against UniRef90.
- The protein database was clustered with Linclust from MMseqs using 90% thresholds for overlap and sequence identity, and online searches are provided against cluster representatives.
Limitations
- Stated: private assembled datasets cannot be brokered into ENA by MGnify, so users must submit assemblies under their own credentials, adding burden; containerization of all pipeline tools for cloud deployment remains ongoing; online sequence similarity searches against the entire protein dataset are not possible due to size, so only cluster representatives are searchable.
- Stated: assembly is computationally expensive and can require terabytes of memory with metaSPAdes; a handful of datasets (<0.1%) could not use metaSPAdes because memory requirements exceeded available maximum.
- Evident from the text: this is a resource and pipeline update rather than a benchmark or validation study, and it does not report accuracy comparisons or independent performance evaluations of the new v5.0 analyses.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
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Cites
Statistics
Claims the paper makes
0 of 16 cited sources checked · 0 supported · 0 flagged
- Findingnone given
MGnify is a free-to-use platform for the assembly, analysis and archiving of microbiome data derived from sequencing microbial populations present in particular environments.
“MGnify (http://www.ebi.ac.uk/metagenomics) provides a free to use platform for the assembly, analysis and archiving of microbiome data derived from sequencing microbial populations that are present in particular environments.”
- Also stated in: § INTRODUCTION · plain
“MGnify (previously known as EBI Metagenomics (14)) is a freely available hub for the analysis, exploration and archiving of microbiome data.”
Quote in the paperNot a substantial claim - Also stated in: § INTRODUCTION · plain
- Findingown data
Over the past two years, MGnify has more than doubled the number of publicly available analysed datasets held within the resource.
“Over the past 2 years, MGnify (formerly EBI Metagenomics) has more than doubled the number of publicly available analysed datasets held within the resource.”
- Also stated in: § UPDATES TO MGnify CONTENT · plain
“This represents a 2-fold increase in the number of datasets analysed over the last two years.”
Quote in the paperNot a substantial claim - Also stated in: § UPDATES TO MGnify CONTENT · plain
- Findingnone given
Biochemical pathways and systems predictions have been added for assembled contigs.
“Biochemical pathways and systems predictions have also been added for assembled contigs.”
Quote in the paperNot a substantial claim - Findingnone given
At the renaming of MGnify in June 2018, unique and stable accession numbers for studies and analyses were introduced, replacing study and run accessions inherited from INSDC.
“At the time of the renaming of resource in June 2018, unique and stable accession numbers for studies and analyses in MGnify were introduced, replacing the study and run accessions, respectively, that were inherited from INSDC.”
Quote in the paperNot a substantial claim - Findingnone given
MGnify version 5.0 replaced the previous single pipeline with multiple analysis pipelines tailored according to input data.
“Recently, an updated approach to data analysis has been unveiled (version 5.0), replacing the previous single pipeline with multiple analysis pipelines that are tailored according to the input data, and that are formally described using the Common Workflow Language, enabling greater provenance, reusability, and reproducibility.”
Quote in the paperSubstantial claim
- Findingreasoning
MGnify's number of datasets assembled and analysed has increased six-fold.
“MGnify's growing focus on the assembly of metagenomic data has also seen the number of datasets it has assembled and analysed increase six-fold.”
Quote in the paperNot a substantial claim - Findingown data
The non-redundant protein database constructed from proteins encoded by MGnify assemblies now exceeds 1 billion sequences.
“The non-redundant protein database constructed from the proteins encoded by these assemblies now exceeds 1 billion sequences.”
Quote in the paperNot a substantial claim - Findingnone given
A newly developed contig viewer provides fine-grained visualisation of assembled contigs and their enriched annotations.
“Meanwhile, a newly developed contig viewer provides fine-grained visualisation of the assembled contigs and their enriched annotations.”
Quote in the paperNot a substantial claim - Findingreasoning
Providing online sequence similarity searches against the entire MGnify protein dataset has not been possible due to the size of the full database.
“Providing online sequence similarity searches against the entire protein dataset has not been possible, due to the size of the full database.”
Quote in the paperSubstantial claim - Findingreasoning
MGnify added the concept of Super Studies to its data model, allowing grouping of related projects under a single entry point.
“To enable this, we have added the concept of ‘Super Studies’ to the MGnify data model, which allows the grouping of related projects under a single entry point.”
Quote in the paperNot a substantial claim - Findingown data
15% of MGnify protein sequences are truncated at either the N or C terminus.
“Approximately 25% of these sequences are predicted to be full length according to Prodigal's gene identification criteria, with 15% truncated at either the N or C terminus and 60% predicted to be truncated at both ends (termed ‘partials’).”
Quote in the paperNot a substantial claim - Findingown data
Approximately one third of these assemblies have been uploaded and analysed with MGnify to date.
“Approximately one third of these assemblies have been uploaded and analysed with MGnify to date (accessible via https://www.ebi.ac.uk/metagenomics/search#analyses, and selecting the ‘Assembly’ facet found under the ‘Experiment Type’ section of facets, listed on the left of the page).”
Quote in the paperNot a substantial claim - Findingnone given
Since assembly of shotgun metagenomics data was introduced to MGnify in 2018, there has been a high uptake of this feature, both for public datasets requested for analysis and for private analysis.
“Since assembly of shotgun metagenomics data was introduced to MGnify in 2018, we have seen a high uptake of this new feature, both in terms of public datasets being requested for analysis and for private analysis.”
Quote in the paperNot a substantial claim - Findingreasoning
Assembled private datasets cannot be brokered into ENA by MGnify on behalf of the submitter.
“However, assembled private datasets can not be brokered into the ENA by MGnify on behalf of the submitter.”
Quote in the paperSubstantial claim - Findingown data
Over the past two years, only a handful of datasets (<0.1%) out of the approximately 43000 assemblies have not been produced using metaSPAdes, due to memory requirements exceeding the maximum available.
“Over the past two years, only a handful of datasets (<0.1%) out of the ∼43 000 assemblies have not been produced using metaSPAdes, due to memory requirements exceeding the maximum available.”
Quote in the paperNot a substantial claim - Findingnone given
The MGnify protein database grew from 50 million sequences (v2017_08) to over 1.1 billion (v2019_05) over the past 2 years.
“Over the past 2 years, this database has grown from 50 million sequences (v2017_08) to over 1.1 billion (v2019_05).”
Quote in the paperNot a substantial claim - Findingown data
60% of MGnify protein sequences are predicted to be truncated at both ends (termed 'partials').
“Approximately 25% of these sequences are predicted to be full length according to Prodigal's gene identification criteria, with 15% truncated at either the N or C terminus and 60% predicted to be truncated at both ends (termed ‘partials’).”
Quote in the paperNot a substantial claim - Study design and conductreasoning
MGnify's analysis pipelines are formally described using Common Workflow Language, enabling greater provenance, reusability, and reproducibility.
“Recently, an updated approach to data analysis has been unveiled (version 5.0), replacing the previous single pipeline with multiple analysis pipelines that are tailored according to the input data, and that are formally described using the Common Workflow Language, enabling greater provenance, reusability, and reproducibility.”
Quote in the paperSubstantial claim - Interpretationreasoning
The updates described in the paper close many of the gaps in MGnify's analysis repertoire through expanded scope of taxonomic and functional analyses, range of data products, and visualizations.
“The updates described here close many of the gaps in its analysis repertoire, through the expanded scope of taxonomic and functional analyses, the range of data products and the visualizations provided by the website.”
Quote in the paperSubstantial claim - Interpretationnone given
The use of CWL increases the ability to deploy the MGnify pipeline in different cloud computing platforms.
“The use of CWL also increases our ability to deploy the pipeline in different cloud computing platforms”
Quote in the paperNot a substantial claim - Premisereasoning
MGnify's data policy requires that all sequence datasets it analyses must be appropriately archived within INSDC.
“Our ambition is to ensure that all of the assemblies generated by MGnify are submitted into the ENA, in line with our data policy that all sequence datasets we analyse must be appropriately archived within INSDC.”
Quote in the paperNot a substantial claim
- Classified as probably not a substantial claim. 22
- May combine two claims. 19
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenMGnify covers studies targeting taxonomic markers such as SSU rRNA gene (amplicon), whole genome shotgun sequencing (metagenomics), and whole transcriptome shotgun sequencing (metatranscriptomics).
“Amongst the data types covered are studies that target taxonomic markers, such as the small subunit (SSU) ribosomal ribonucleic acid gene (amplicon studies), whole genome shotgun sequencing studies (metagenomics) and whole transcriptome shotgun sequencing studies (metatranscriptomics).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationThrough partnership with ENA, sequencing data and metadata submitted for analysis are accessioned and stored permanently within the archive, which operates under INSDC.
“Through partnership with the ENA, sequencing data and metadata submitted for analysis are accessioned and stored permanently within the archive, which operates under the International Nucleotide Sequence Database Collaboration (INSDC) (15).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [15] Karsch-Mizrachi, 2018, The international nucleotide sequence database collaboration, Nucleic Acids Res. source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenIn MGnify, analysis of user-submitted data is supplemented by processing publicly available microbiome datasets drawn from INSDC via ENA.
“In MGnify, analysis of user-submitted data is supplemented by processing publicly available microbiome datasets drawn from the INSDC via the ENA.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Findingnone givenMGnify accepts user-submitted data and provides standardized pipelines that offer taxonomic and, where appropriate, functional analysis of microbiome datasets.
“The resource accepts user-submitted data and provides standardized pipelines that offer taxonomic and (where appropriate) functional analysis of microbiome datasets.”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationMGnify curators add supplementary metadata to imported studies, assigning a relevant biome selected from GOLD biosample hierarchy.
“The distinction between MGnify studies and ENA projects is important, as MGnify curators add supplementary metadata to imported studies, assigning a relevant biome selected from the Genomes OnLine Database (GOLD) (17) biosample hierarchy.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [17] Mukherjee, 2019, Genomes OnLine database (GOLD) v.7: updates and new features, Nucleic Acids Res. source
Not checked in the free run.
May combine two claims.
Findingnone givenMGnify's new analysis pipelines offer additional approaches for taxonomic assertions based on ribosomal internal transcribed spacer regions (ITS1/2) and expanded protein functional annotations.
“MGnify's new analysis pipelines offer additional approaches for taxonomic assertions based on ribosomal internal transcribed spacer regions (ITS1/2) and expanded protein functional annotations.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingnone givenMGnify analyses reside within MGnify, which provides an independent website and API for data discovery and exploration.
“Meanwhile, the analyses of these datasets (both pre-release and publicly available) reside within MGnify, which provides an independent website and API for data discovery and exploration.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenMGnify users can request that any relevant publicly available study found within INSDC can be analysed with the latest MGnify pipeline version, and the results added to the resource.
“Furthermore, MGnify users can request that any relevant publicly available study found within the INSDC can be analysed with the latest MGnify pipeline version, and the results added to the resource.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingnone givenMGnify has begun to offer analysis of user-submitted assembled sequence data and/or can provide assembly of user-submitted metagenomic data prior to analysis (available upon request).
“More recently, the resource has begun to offer analysis of user-submitted assembled sequence data (assembly), and/or can provide assembly of user-submitted metagenomic data prior to analysis (available upon request).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataTo date, MGnify has assembled approximately 43000 sequencing runs drawn from a wide range of biomes, and is in the process of submitting the assembled contigs back into ENA.
“To date, we have assembled ∼43 000 sequencing runs drawn from a wide range of biomes, and are in the process of submitting the assembled contigs back into the ENA.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenSince the first inception of the analysis pipeline in 2011, there have been five major versions.
“Since the first inception of the analysis pipeline in 2011, there have been five major versions.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
FindingcitationAdditional functional analyses are provided in the form of KEGG orthologue annotations, calculated using HMMER and the KOfam library on predicted protein sequences.
“Additional functional analyses are also provided in the form of KEGG orthologue (KO) (23) annotations, which are calculated using HMMER (40) and the KOfam library (using a slightly modified form of the profile hidden Markov model (HMM) database of KEGG orthologues (41)) on the predicted protein sequences.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [23] Kanehisa, 2016, KEGG as a reference resource for gene and protein annotation, Nucleic Acids Res. source
Not checked in the free run.
- cites [40] Eddy, 2011, Accelerated Profile HMM Searches, PLoS Comput. Biol. source
Not checked in the free run.
- cites [41] Aramaki, 2019, KofamKOALA: KEGG ortholog assignment based on profile HMM and adaptive score threshold source
Not checked in the free run.
May combine two claims.
Findingown dataOnly 9 million identical sequences are in common between MGnify and UniProtKB, indicating very little overlap.
“Despite the substantial increase in number, there remains very little overlap with the sequences found in MGnify and those in UniProtKB, with only 9 million identical sequences in common between the two resources.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Findingnone givenThe different proportions of analyses (amplicon, metagenomics and assembled) closely reflect the corresponding proportions of raw sequence data found in ENA.
“The different proportions of analyses (amplicon, metagenomics and assembled) closely reflect the corresponding proportions of raw sequence data found in ENA.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationMGnify's latest update v5.0, released September 2019, extends analyses further, substantially increasing the scope of functional annotations through the addition of KEGG orthologue predictions for reads and assembled contigs, and KEGG pathways and Genome Properties annotations for assembled contigs.
“The latest update (v5.0), released September 2019, extends the analyses further, substantially increasing the scope of functional annotations through the addition of KEGG (23) orthologue predictions for reads and assembled contigs, and KEGG pathways and Genome Properties (24) annotations for assembled contigs.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [23] Kanehisa, 2016, KEGG as a reference resource for gene and protein annotation, Nucleic Acids Res. source
Not checked in the free run.
- cites [24] Richardson, 2019, Genome properties in 2019: a new companion database to InterPro for the inference of complete functional attributes, Nucleic Acids Res. source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataApproximately 25% of MGnify protein sequences are predicted to be full length according to Prodigal's gene identification criteria.
“Approximately 25% of these sequences are predicted to be full length according to Prodigal's gene identification criteria, with 15% truncated at either the N or C terminus and 60% predicted to be truncated at both ends (termed ‘partials’).”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe majority of MGnify data are 16S or 18S rRNA gene amplicon datasets, followed by metagenomic and assembly analyses, with smaller numbers of metatranscriptomes and metabarcoding runs.
“The majority of this data (∼193 000 analyses) are 16S or 18S rRNA gene amplicon datasets, followed by metagenomic (∼27 000) and assembly (∼16 000) analyses, with a smaller number of analysed metatranscriptomes (∼2000) and metabarcoding runs (∼2000, the majority of which target internally transcribed spacer (ITS) regions - as previous pipelines could not analyse ITS regions, these datasets will be”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
FindingreasoningDue to the clustering parameters, the selected cluster representative (centroid sequence) is typically the longest.
“Due to the clustering parameters, the selected cluster representative (the centroid sequence), is typically the longest.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
FindingcitationAt present, all 96 individual studies that make up the Earth Microbiome Project are grouped together under a single Super Study, as are MGnify analyses for 8 distinct Tara Oceans datasets.
“For example, at present, all 96 individual studies that make up the Earth Microbiome Project (18) are grouped together under a single Super Study, as are MGnify analyses for 8 distinct Tara Oceans (19) datasets.”
Quote in the paperNot a substantial claim0 of 2 sources checkedMay combine two claims.
Findingown dataMGnify currently contains over 3500 publicly available projects, comprising approximately 175000 samples, 230000 runs and 240000 analyses.
“In terms of overall data, MGnify currently contains over 3500 publicly available projects, comprising ∼175 000 samples, ∼230 000 runs and ∼240 000 analyses.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenIn version 5.0, analysis of amplicon datasets has been expanded from SSU and LSU-based classifications to include those based on ITS regions.
“In version 5.0 of the pipeline, analysis of amplicon datasets has been expanded from SSU and LSU-based classifications to include those based on ITS regions.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationThe new MGnify pipeline defined the CWL workflow first and utilizes toil-cwl-runner to orchestrate execution on their compute infrastructure.
“The new pipeline is a major departure from this practice, where we have defined the CWL workflow first, and now utilize toil-cwl-runner (a CWL compatibility layer that is a part of the Toil workflow execution engine (26)) to orchestrate the execution on our compute infrastructure.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [26] Vivian, 2017, Toil enables reproducible, open source, big biomedical data analyses, Nat. Biotechnol. source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
FindingreasoningPfam annotations are now provided as an additional results set to aid comparison with other resources that use Pfam for annotation, such as IMG/M.
“While previously available as part of the InterPro results, Pfam (39) annotations are now provided as an additional results set to aid comparison with other resources that use Pfam for annotation, such as IMG/M.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [39] El-Gebali, 2019, The Pfam protein families database in 2019, Nucleic Acids Res. source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
FindingreasoningThe two ITS reference databases (ITSoneDB and UNITE) offer complementary coverage.
“The two ITS reference databases offer complementary coverage.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
InterpretationreasoningEnabling large scale data analysis using standardized pipelines allows studies to be placed in context with each other, increasing data reuse and maximizing knowledge extracted from datasets.
“Enabling large scale data analysis using standardized pipelines in this way allows studies to be placed in context with each other, increasing data reuse and maximizing the knowledge that can be extracted from the datasets.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationreasoningThe introduction of unique stable accession numbers allows users to distinguish analysed microbiome datasets from primary sequence data in ENA and helps identify where MGnify adds content.
“Driven by ongoing efforts to adhere to the FAIR data principles (16) (aimed to make data findable, accessible, interoperable and reusable), this change allows users to distinguish analysed microbiome datasets from the primary sequence data in ENA - which continue to be presented under the study and run accessions - and helps identify where MGnify adds content.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [16] Wilkinson, 2016, The FAIR Guiding Principles for scientific data management and stewardship, Sci. Data source
Not checked in the free run.
May combine two claims.
Study design and conductreasoningDefining the CWL workflow first and using toil-cwl-runner removed duplication of effort and helps ensure provenance, interoperability and reproducibility of the pipeline.
“This has removed the duplication of effort (in terms of implementing the logic in software and then retrospectively producing a CWL description), and helps ensure provenance, interoperability and reproducibility of the pipeline.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenThe adoption of third party workflow execution engines reduces the burden for maintaining pipelining software.
“The adoption of third party workflow execution engines reduces the burden for maintaining pipelining software”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningKEGG pathways and Genome Properties annotations represent higher order annotations (based on two or more proteins) that enable the description of functional systems encoded by the microbes within a metagenome.
“The latter two represent higher order annotations (based on two or more proteins) that enable the description of functional systems encoded by the microbes within a metagenome.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductcitationAdditional phylogenetic marker gene-based operational taxonomic unit profiling is performed using mOTUs2 on all reads that pass QC, which allows sensitive and accurate quantification for both known and unknown species.
“Additional phylogenetic marker gene-based operational taxonomic unit profiling is performed using mOTUs2 (35) on all reads that pass QC, which allows sensitive and accurate quantification for both known and unknown species.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [35] Milanese, 2019, Microbial abundance, activity and population genomic profiling with mOTUs2, Nat. Commun. source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationMetagenomics has provided the scientific community with access to approximately 99% of organisms that are yet to be cultured.
“Metagenomics has started to provide the scientific community with access to the ∼99% of organisms that are yet to be cultured (50).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [50] Rinke, 2013, Insights into the phylogeny and coding potential of microbial dark matter, Nature source
Not checked in the free run.
Classified as probably not a substantial claim.
InterpretationreasoningThe Super Studies facility makes it easier to discover, explore and compare data across large-scale projects.
“The Super Studies facility makes it easier to discover, explore and compare data across such large-scale projects.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S4 (based). May combine two claims.
Interpretationnone givenAssembly of reads into longer contigs can underpin a deeper understanding of the data through recovery of full-length proteins, prediction of complete biochemical pathways and/or biological systems, and potential reconstruction of complete genomes.
“Whilst analysis of raw reads can provide detailed insights into the microbiome, assembly of the reads into longer contigs can underpin a deeper understanding of the data through recovery of full-length proteins, prediction of complete biochemical pathways and/or biological systems, and potential reconstruction of complete genomes.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductcitationmetaSPAdes is MGnify's primary assembly algorithm because the ensuing assemblies are typically of better quality than those produced using other assemblers.
“Assembly is a computationally expensive process, frequently requiring terabytes of memory to accomplish when using metaSPAdes (20), which is our primary assembly algorithm, as the ensuing assemblies are typically of better quality than those produced using other assemblers (21).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [20] Nurk, 2017, metaSPAdes: a new versatile metagenomic assembler, Genome Res. source
Not checked in the free run.
- cites [21] Vollmers, 2017, Comparing and evaluating metagenome assembly tools from a microbiologist's perspective - not only size matters!, PLoS One source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenThese updates have particularly improved the interpretation of metagenomics assemblies.
“Notably, these have particularly improved the interpretation of metagenomics assemblies.”
Quote in the paperNot a substantial claim- Rests on an assumption: The assembled data provides a deeper understanding of microbiomes, providing access to full length proteins, enabling the assertion of pathways and systems, and is foundational to the reconstruction of genomes.
The paper relies on this without support.
MGnify is one of the world's largest resources for the analysis of microbiome datasets.
“MGnify is one of the world's largest resources for the analysis of microbiome datasets.”
The paper relies on this without support.
MGnify and IMG/M are the only major resources offering metagenomic assembly as a service.
“To our knowledge, MGnify and IMG/M are the only major resources offering metagenomic assembly as a service, with both having large, inequivalent collections of metagenomics assemblies.”
The paper relies on this without support.
The assembled data provides a deeper understanding of microbiomes, providing access to full length proteins, enabling the assertion of pathways and systems, and is foundational to the reconstruction of genomes.
“While assembly of large shotgun metagenomics datasets remains computationally expensive, the assembled data (potentially) provides a deeper understanding of microbiomes, providing access to full length proteins, enabling the assertion of pathways and systems, and are foundational to the reconstruction of genomes (i.e. metagenome assembled genomes, known as ‘MAGs’).”
The paper relies on this without support.
Understanding the genomic context of proteins can provide greater insights into their functional roles.
“However, understanding the genomic context of proteins can provide greater insights into their functional roles.”
The paper relies on this without support.
A metagenomics assembly may typically contain more than 1000 contigs.
“As a metagenomics assembly may typically contain >1000 contigs, a range of parameters can be selected to filter the results.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The paper folds over 617 million sequences from the MGnify90 database.
“We fold over 617 million sequences from the MGnify90 database (25).”
From Evolutionary-scale prediction of atomic level protein structure with a language model (2022) · cites this paper as [25]
The 'UPDATES TO THE MGnify PROTEIN DATABASE' section describes MGnify protein sequences clustered at 90% identity, supporting the identification of the database. It reports over 1.1 billion sequences in the full database, but does not give a count of 617 million for the 90%-clustered set. The citing authors' folding of those sequences is their own work, not a finding attributed to this source. (LLM, conf=0.84)
Experimental — accuracy not yet measuredThe ESM Metagenomic Atlas is the first large-scale structural characterization of metagenomic proteins, with more than 617 million structures, folding practically all sequences in MGnify90.
“This is the first large-scale structural characterization of metagenomic proteins, with more than 617 million structures.”
From Evolutionary-scale prediction of atomic level protein structure with a language model (2022) · cites this paper as [25]
The ‘UPDATES TO THE MGnify PROTEIN DATABASE’ section describes more than 1.1 billion protein sequences and their clustering, not predicted structures. Searches for the ESM Metagenomic Atlas, 617 million structures, and protein folding found no passage addressing the claimed structural characterization. (LLM, conf=0.76)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
SeqPrep citation points to an AdapterRemoval paper
MinorThe amplicon-pipeline description cites reference 27 for SeqPrep, but reference 27 is a paper about AdapterRemoval.
“paired end sequences are merged with SeqPrep (v1.2) (27)”
“27. Lindgreen S. AdapterRemoval: easy cleaning of next-generation sequencing reads. BMC Res. Notes. 2012; 5: 337– 337. 22748135 PMC3532080”
Cites
Trimmomatic: a flexible trimmer for Illumina sequence data
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KEGG as a reference resource for gene and protein annotation
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Accelerated Profile HMM Searches
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The Pfam protein families database in 2019
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Self-citationmetaSPAdes: a new versatile metagenomic assembler
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Fast Genome-Wide Functional Annotation through Orthology Assignment by eggNOG-Mapper
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A communal catalogue reveals Earth's multiscale microbial diversity
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Self-citationToil enables reproducible, open source, big biomedical data analyses
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A new genomic blueprint of the human gut microbiota
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Self-citationMapping human microbiome drug metabolism by gut bacteria and their genes
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antiSMASH 4.0—improvements in chemistry prediction and gene cluster boundary identification
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Self-citationGlobal diversity and biogeography of bacterial communities in wastewater treatment plants
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Clustering huge protein sequence sets in linear time
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FragGeneScan: predicting genes in short and error-prone reads
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New insights from uncultivated genomes of the global human gut microbiome
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The International Nucleotide Sequence Database Collaboration
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Self-citationAdapterRemoval: easy cleaning of next-generation sequencing reads
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A holistic approach to marine eco-systems biology
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Microbial abundance, activity and population genomic profiling with mOTUs2
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“Additional phylogenetic marker gene-based operational taxonomic unit profiling is performed using mOTUs2 (35) on all reads that pass QC, which allows sensitive and accurate quantification for both known and unknown species.”
Vollmers, J., Wiegand, S., & Kaster, A.-K. (2017) · PLoS ONE · doi:10.1371/journal.pone.0169662 · Cited by 240 · see citing works
Phylogenetic Diversity and Metabolic Potential Revealed in a Glacier Ice Metagenome
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Genomes OnLine database (GOLD) v.7: updates and new features
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Mitchell, A., Scheremetjew, M., Denise, H., Potter, S., Tarkowska, A., Qureshi, M., Salazar, G. A., Pesseat, S., Boland, M. A., Hunter, F. M. I., et al. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx967 · Cited by 208 · see citing works
Self-citationProliferation of hydrocarbon-degrading microbes at the bottom of the Mariana Trench
Liu, J., Zheng, Y., Lin, H., Wang, X., Li, M., Liu, Y., Yu, M., Zhao, M., Pedentchouk, N., Lea‐Smith, D. J., et al. (2019) · Microbiome · doi:10.1186/s40168-019-0652-3 · Cited by 193 · see citing works
The international nucleotide sequence database collaboration
Karsch-Mizrachi, I., Takagi, T., Cochrane, G., & on behalf of the International Nucleotide Sequence Database Collaboration (2018) · Nucleic Acids Research · doi:10.1093/nar/gkx1097 · Cited by 190 · see citing works
Self-citationMAPseq: highly efficient k-mer search with confidence estimates, for rRNA sequence analysis
Rodrigues, J. F. M., Schmidt, T., Tackmann, J., & von Mering, C. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btx517 · Cited by 181 · see citing works
Microbial diversity and soil physiochemical characteristic of higher altitude
Kumar, S., Suyal, D. C., Yadav, A., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213844 · Cited by 181 · see citing works
The European Nucleotide Archive in 2018
Harrison, P. W., Alako, B., Amid, C., Cerdeño-Tárraga, A. M., Cleland, I., Holt, S., Hussein, A., Jayathilaka, S., Kay, S., Keane, T., et al. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1078 · Cited by 115 · see citing works
Self-citationKhan, F. Z., Soiland‐Reyes, S., Sinnott, R., Lonie, A. J., Goble, C., & Crusoe, M. R. (2019) · GigaScience · doi:10.1093/gigascience/giz095 · Cited by 86 · see citing works
Self-citationThe metagenomic data life-cycle: standards and best practices
ten Hoopen, P., FINN, R., Bongo, L. A., et al. (2017) · GigaScience · doi:10.1093/gigascience/gix047 · Cited by 72 · see citing works
Self-citationSantamaría, M., Fosso, B., Licciulli, F., Balech, B., Larini, I., Grillo, G., Caro, G. D., Liuni, S., & Pesole, G. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx855 · Cited by 43 · see citing works
Richardson, L. J., Rawlings, N. D., Salazar, G. A., Almeida, A., Haft, D. R., Ducq, G., Sutton, G. G., & Finn, R. D. (2019) · Nucleic Acids Research · doi:10.1093/nar/gky1013 · Cited by 36 · see citing works
Self-citationHaines, S. R., Bope, A., Horack, J. M., Meyer, M. E., & Dannemiller, K. C. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-10053-4 · Cited by 21 · see citing works
Microbial community composition and diversity in the Indian Ocean deep sea REY-rich muds
Wang, S., Yu, M., Wei, J., et al. (2018) · PLoS ONE · doi:10.1371/journal.pone.0208230 · Cited by 17 · see citing works
Overholt, W. A., Schwing, P., Raz, K. M., Hastings, D. W., Hollander, D. J., & Kostka, J. E. (2019) · Environmental Microbiology · doi:10.1111/1462-2920.14794 · Cited by 13 · see citing works
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Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764 · see citing works
“Through an enormous experimental effort 1–4 , the structures of around 100,000 unique proteins have been determined 5 , but this represents a small fraction of the billions of known protein sequences 6,7 .”
ColabFold - Making protein folding accessible to all
Mirdita, M., Schütze, K., Moriwaki, Y., Heo, L., Ovchinnikov, S., & Steinegger, M. (2021) · doi:10.1101/2021.08.15.456425 · Cited by 9,391 · see citing works
The PRIDE database resources in 2022: a hub for mass spectrometry-based proteomics evidences
Perez-Riverol, Y., Bai, J., Bandla, C., García-Seisdedos, D., Hewapathirana, S., Kamatchinathan, S., Kundu, D. J., Prakash, A., Frericks-Zipper, A., Eisenacher, M., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkab1038 · Cited by 6,125 · see citing works
Evolutionary-scale prediction of atomic level protein structure with a language model
Lin, Z., Akin, H., Rao, R., Hie, B., Zhu, Z., Lu, W., Smetanin, N., Verkuil, R., Kabeli, O., Shmueli, Y., et al. (2022) · doi:10.1101/2022.07.20.500902 · Cited by 5,523 · see citing works
Protein complex prediction with AlphaFold-Multimer
Evans, R., O’Neill, M., Pritzel, A., Antropova, N., Senior, A., Green, T., Žídek, A., Bates, R., Blackwell, S., Yim, J., et al. (2021) · doi:10.1101/2021.10.04.463034 · Cited by 3,808 · see citing works
Parks, D. H., Chuvochina, M., Rinke, C., Mussig, A. J., Chaumeil, P.-A., & Hugenholtz, P. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkab776 · Cited by 2,402 · see citing works
A unified catalog of 204,938 reference genomes from the human gut microbiome
Almeida, A., Nayfach, S., Boland, M., Strozzi, F., Beracochea, M., Shi, Z. J., Pollard, K. S., Sakharova, E., Parks, D. H., Hugenholtz, P., et al. (2021) · Nature Biotechnology · doi:10.1038/s41587-020-0603-3 · Cited by 1,367 · see citing works
Self-citationImproved prediction of protein-protein interactions using AlphaFold2
Bryant, P., Pozzati, G., & Elofsson, A. (2021) · doi:10.1101/2021.09.15.460468 · Cited by 1,025 · see citing works
Using machine learning approaches for multi-omics data analysis: A review
Reel, P. S., Reel, S., Pearson, E., Trucco, E., & Jefferson, E. (2021) · Biotechnology Advances · doi:10.1016/j.biotechadv.2021.107739 · Cited by 903 · see citing works
Metagenomic compendium of 189,680 DNA viruses from the human gut microbiome
Nayfach, S., Páez-Espino, D., Call, L., Low, S. J., Sberro, H., Ivanova, N. N., Proal, A. D., Fischbach, M. A., Bhatt, A. S., Hugenholtz, P., et al. (2021) · Nature Microbiology · doi:10.1038/s41564-021-00928-6 · Cited by 580 · see citing works
Sequence modeling and design from molecular to genome scale with Evo
Nguyen, E., Poli, M., Durrant, M. G., Kang, B., Katrekar, D., Li, D. B., Bartie, L. J., Thomas, A. W., King, S. H., Brixi, G., et al. (2024) · Science · doi:10.1126/science.ado9336 · Cited by 580 · see citing works
The food-gut axis: lactic acid bacteria and their link to food, the gut microbiome and human health
De Filippis, F., Pasolli, E., & Ercolini, D. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa015 · Cited by 303 · see citing works
Protein structure predictions to atomic accuracy with AlphaFold
Jumper, J., & Hassabis, D. (2022) · Nature Methods · doi:10.1038/s41592-021-01362-6 · Cited by 265 · see citing works
AF2Complex predicts direct physical interactions in multimeric proteins with deep learning
Gao, M., Nakajima An, D., Parks, J. M., & Skolnick, J. (2022) · Nature Communications · doi:10.1038/s41467-022-29394-2 · Cited by 252 · see citing works
SPEACH_AF: Sampling protein ensembles and conformational heterogeneity with Alphafold2
Stein, R. A., & Mchaourab, H. S. (2022) · PLOS Computational Biology · doi:10.1371/journal.pcbi.1010483 · Cited by 258 · see citing works
Beresford-Jones, B. S., Forster, S. C., Stares, M. D., Notley, G., Viciani, E., Browne, H. P., Boehmler, D. J., Soderholm, A. T., Kumar, N., Vervier, K., et al. (2022) · Cell Host & Microbe · doi:10.1016/j.chom.2021.12.003 · Cited by 194 · see citing works
Self-citationBridge RNAs direct programmable recombination of target and donor DNA
Durrant, M. G., Perry, N. T., Pai, J. J., Jangid, A. R., Athukoralage, J. S., Hiraizumi, M., McSpedon, J. P., Pawluk, A., Nishimasu, H., Konermann, S., et al. (2024) · Nature · doi:10.1038/s41586-024-07552-4 · Cited by 163 · see citing works
AlphaFold2-aware protein–DNA binding site prediction using graph transformer
Yuan, Q., Chen, S., Rao, J., Zheng, S., Zhao, H., & Yang, Y. (2022) · Briefings in Bioinformatics · doi:10.1093/bib/bbab564 · Cited by 137 · see citing works
Novel machine learning approaches revolutionize protein knowledge
Bordin, N., Dallago, C., Heinzinger, M., Kim, S., Littmann, M., Rauer, C., Steinegger, M., Rost, B., & Orengo, C. (2023) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2022.11.001 · Cited by 72 · see citing works
Protein sequence‐to‐structure learning: Is this the end(‐to‐end revolution)?
Laine, E., Eismann, S., Elofsson, A., & Grudinin, S. (2021) · Proteins: Structure, Function, and Bioinformatics · doi:10.1002/prot.26235 · Cited by 44 · see citing works
“They include databases like NCBI GenBank [66], Metaclust [67], BFD [68], MetaEuk [69], EBI MGnify [70], and IMG/M [71].”
MethodToward a health-associated core keystone index for the human gut microbiome
Goel, A., Shete, O., Goswami, S., Samal, A., C.B., L., Kedia, S., Ahuja, V., O’Toole, P. W., Shanahan, F., & Ghosh, T. S. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115378 · Cited by 37 · see citing works
Deep learning and CRISPR-Cas13d ortholog discovery for optimized RNA targeting
Wei, J., Lotfy, P., Faizi, K., Baungaard, S., Gibson, E., Wang, E., Slabodkin, H., Kinnaman, E., Chandrasekaran, S., Kitano, H., et al. (2021) · doi:10.1101/2021.09.14.460134 · Cited by 67 · see citing works
Zhang, Y., Zhang, Z., Kagaya, Y., Terashi, G., Zhao, B., Xiong, Y., & Kihara, D. (2025) · Communications Biology · doi:10.1038/s42003-025-08783-5 · Cited by 19 · see citing works
Parente, E., Zotta, T., & Ricciardi, A. (2022) · doi:10.1101/2022.01.19.476946 · Cited by 15 · see citing works
- Authors
- Mitchell, A. L., Almeida, A., Beracochea, M., Boland, M., Burgin, J., Cochrane, G., Crusoe, M. R., Kale, V., Potter, S. C., Richardson, L. J., Sakharova, E., Scheremetjew, M., Korobeynikov, A., Shlemov, A., Kunyavskaya, O., Lapidus, A., & Finn, R. D.
- Affiliations
- European Bioinformatics Institute (GB)
- European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK
- Common Workflow Language, a project of the Software Freedom Conservancy, Inc. 137 Montague Street, Suite 380, Brooklyn, NY 11201-3548, USA
- St Petersburg University (RU)
- Center for Algorithmic Biotechnologies, Saint Petersburg State University, Russia
- Corresponding author
- Finn, Robert D
- ORCID
- Venue
- Nucleic Acids Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2019-11-07
- Volume
- 48
- Issue
- D1
- Pages
- D570-D578
- ISSN
- 0305-1048 (ISSN-L)
- 1362-4962
- PMC
- PMC7145632
- OpenAlex
- W2984894304
- Semantic Scholar
- 633155ae06b2367cc42d5beb21d2be85330b6200
- Cited by
- 562
- References
- 53
- Citations by year
- 2026: 23 · 2025: 68 · 2024: 100 · 2023: 112 · 2022: 131 · 2021: 95 · 2020: 30 · 2019: 2
- FWCI
- 21.33
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Nucleic Acids Research (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Horizon 2020 (676559, 817729)
- Biotechnology and Biosciences Research Council (BB/M011755/1, BB/R015228/1, BB/N018354/1)
- ELIXIR
- Russian Fund for Basic Research (18-54-74004)
- European Molecular Biology Laboratory
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Social Sciences › Decision Sciences › Information Systems and Management › Scientific Computing and Data Management
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Keywords
- MGnify, metagenome assembly, data analysis pipeline, Common Workflow Language, reproducibility, taxonomic annotation, ITS1-2, protein annotation, microbial communities
- MeSH terms
- Archaea, Bacteria, Phylogeny, Software, DNA, Ribosomal Spacer, Databases, Genetic, Metagenome, Metagenomics, Microbiota
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-10.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-10.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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