Evidence map›Paper›PMID 38868716›Full record

ArticleiMeta2022

Are short-read amplicons suitable for the prediction of microbiome functional potential? A critical perspective.

Vitor Heidrich, Lukas Beule

Abstract read
In one paragraph

Article in iMeta, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. TwoInternational journal of molecular sciences · 2026
    Article
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  5. Review
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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

2 authors.

Vitor HeidrichCentro de Oncologia Molecular Hospital Sírio-Libanês São Paulo Brazil.ORCID https://orcid.org/0000-0001-6617-9187
Lukas BeuleJulius Kühn Institute (JKI)-Federal Research Centre for Cultivated Plants Institute for Ecological Chemistry, Plant Analysis and Stored Product Protection Berlin Germany.ORCID https://orcid.org/0000-0003-1107-7540

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Taxonomic marker gene analysis allows uncovering taxonomic profiles of microbial communities at low cost, making it omnipresent in microbiome research. There is an ever-expanding set of tools to extract further biological information from this kind of data. In this perspective, we enunciate several concerns regarding the biological validity of predicting functional potential from taxonomic profiles, especially when they are generated by short-read sequencing. The taxonomic resolution of marker genes, intragenomic variability of marker genes, and the compositional nature of microbiome data are discussed. Combining actual measurements of microbiome functions with predicted functional potentials is proposed as a powerful approach to better understand microbiome functioning. In this context, the significance of predicted functional potentials for generating and testing hypotheses is highlighted. We argue that functions of microbiomes predicted from microbiome DNA read count data generated by short-read amplicon sequencing should not serve as the only basis to draw biological inferences.

Indexed as

compositional datafunctional potential profilesintragenomic marker gene variabilitymicrobial functionsmicrobiome datashort‐read amplicon sequencingtaxonomic resolution

Identifiers

PMID38868716
PMCPMC10989910

What OpenQuestion holds

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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.