Evidence map›Paper›PMID 29858539›Full record

ArticleMolecular ecology2019

Counting with DNA in metabarcoding studies: How should we convert sequence reads to dietary data?

Bruce E Deagle, Austen C Thomas, Julie C McInnes, Laurence J Clarke, Eero J Vesterinen, Elizabeth L Clare, Tyler R Kartzinel, J Paige Eveson

Abstract read
In one paragraph

Article in Molecular ecology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 262 papers.

0numbers the graph read from it
0cells of the map it votes in
262citing 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

262 citing papers in PubMed.

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  20. Habitat-Associated Dietary Plasticity in the Japanese Weasel (Animals : an open access journal from MDPI · 2026
    Article

202 more citing papers are in PubMed but not listed here.

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

8 authors.

Bruce E DeagleAustralian Antarctic Division, Channel Highway, Kingston, TAS, Australia.ORCID 0000-0001-7651-3687
Austen C ThomasScience Department, Smith-Root Inc., Vancouver, Washington.
Julie C McInnesAustralian Antarctic Division, Channel Highway, Kingston, TAS, Australia.ORCID 0000-0001-8902-5199
Laurence J ClarkeAustralian Antarctic Division, Channel Highway, Kingston, TAS, Australia.ORCID 0000-0002-0844-4453
Eero J VesterinenBiodiversity Unit and Department of Biology, University of Turku, Turku, Finland.ORCID 0000-0003-3665-5802
Elizabeth L ClareSchool of Biological and Chemical Sciences, Queen Mary University of London, London, UK.ORCID 0000-0002-6563-3365
Tyler R KartzinelDepartment of Ecology and Evolutionary Biology, Brown University, Providence, Rhode Island.
J Paige EvesonCSIRO Oceans and Atmosphere, Hobart, TAS, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in DNA sequencing technology have revolutionized the field of molecular analysis of trophic interactions, and it is now possible to recover counts of food DNA sequences from a wide range of dietary samples. But what do these counts mean? To obtain an accurate estimate of a consumer's diet should we work strictly with data sets summarizing frequency of occurrence of different food taxa, or is it possible to use relative number of sequences? Both approaches are applied to obtain semi-quantitative diet summaries, but occurrence data are often promoted as a more conservative and reliable option due to taxa-specific biases in recovery of sequences. We explore representative dietary metabarcoding data sets and point out that diet summaries based on occurrence data often overestimate the importance of food consumed in small quantities (potentially including low-level contaminants) and are sensitive to the count threshold used to define an occurrence. Our simulations indicate that using relative read abundance (RRA) information often provides a more accurate view of population-level diet even with moderate recovery biases incorporated; however, RRA summaries are sensitive to recovery biases impacting common diet taxa. Both approaches are more accurate when the mean number of food taxa in samples is small. The ideas presented here highlight the need to consider all sources of bias and to justify the methods used to interpret count data in dietary metabarcoding studies. We encourage researchers to continue addressing methodological challenges and acknowledge unanswered questions to help spur future investigations in this rapidly developing area of research.

Indexed as

DietFood ChainComputer SimulationDNA Barcoding, TaxonomicFecesHigh-Throughput Nucleotide Sequencing

Identifiers

PMID29858539
PMCPMC6905394

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Registered trials

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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.