Evidence map›Paper›PMID 30779309›Full record

ArticleMolecular ecology resources2019

Metabarcoding a diverse arthropod mock community.

Thomas W A Braukmann, Natalia V Ivanova, Sean W J Prosser, Vasco Elbrecht, Dirk Steinke, Sujeevan Ratnasingham, Jeremy R de Waard, Jayme E Sones, Evgeny V Zakharov, Paul D N Hebert

Abstract read
In one paragraph

Article in Molecular ecology resources, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

54 citing papers in PubMed.

  1. Article
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  3. Accuracy of occurrence and abundance estimates from insect metabarcoding.bioRxiv : the preprint server for biology · 2026
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  13. PROTAX-GPU: a scalable probabilistic taxonomic classification system for DNA barcodes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  14. Three steps towards comparability and standardization among molecular methods for characterizing insect communities.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  15. Article
  16. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Thomas W A BraukmannCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.ORCID https://orcid.org/0000-0002-2452-3776
Natalia V IvanovaCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.
Sean W J ProsserCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.
Vasco ElbrechtCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.ORCID https://orcid.org/0000-0003-4672-7099
Dirk SteinkeCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.ORCID http://orcid.org/0000-0002-8992-575X
Sujeevan RatnasinghamCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.
Jeremy R de WaardCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.
Jayme E SonesCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.
Evgeny V ZakharovCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.
Paul D N HebertCentre for Biodiversity Genomics, University of Guelph, Guelph, Ontario, Canada.

Funding

Ministry of Research, Innovation and Science
6 · The paper itself

Abstract

Although DNA metabarcoding is an attractive approach for monitoring biodiversity, it is often difficult to detect all the species present in a bulk sample. In particular, sequence recovery for a given species depends on its biomass and mitome copy number as well as the primer set employed for PCR. To examine these variables, we constructed a mock community of terrestrial arthropods comprised of 374 species. We used this community to examine how species recovery was impacted when amplicon pools were constructed in four ways. The first two protocols involved the construction of bulk DNA extracts from different body segments (Bulk Abdomen, Bulk Leg). The other protocols involved the production of DNA extracts from single legs which were then merged prior to PCR (Composite Leg) or PCR-amplified separately (Single Leg) and then pooled. The amplicons generated by these four treatments were then sequenced on three platforms (Illumina MiSeq, Ion Torrent PGM and Ion Torrent S5). The choice of sequencing platform did not substantially influence species recovery, although the Miseq delivered the highest sequence quality. As expected, species recovery was most efficient from the Single Leg treatment because amplicon abundance varied little among taxa. Among the three treatments where PCR occurred after pooling, the Bulk Abdomen treatment produced a more uniform read abundance than the Bulk Leg or Composite Leg treatment. Primer choice also influenced species recovery and evenness. Our results reveal how variation in protocols can have substantial impacts on perceived diversity unless sequencing coverage is sufficient to reach an asymptote.

Indexed as

MetagenomeAnimalsArthropodsDNADNA Barcoding, TaxonomicModels, TheoreticalSequence Analysis, DNADNAcommunity ecologyDNA barcodingecological geneticsenvironmental DNA

Identifiers

PMID30779309
PMCPMC6850013

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.