Evidence map›Paper›PMID 34737726›Full record

ArticleFrontiers in microbiology2021

Compositional Data Analysis of Microbiome and Any-Omics Datasets: A Validation of the Additive Logratio Transformation.

Michael Greenacre, Marina Martínez-Álvaro, Agustín Blasco

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
–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

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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

62 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  12. Annual Dynamics of Mycobiota in Symptomatic Century-Old Trees ofJournal of fungi (Basel, Switzerland) · 2026
    Article
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  15. Frontiers in microbiology · 2026
    Article
  16. Review
  17. SIMBA-GNN: mechanistic graph learning for microbiome prediction.NPJ systems biology and applications · 2025
    Article
  18. Article
  19. Article
  20. Article

2 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

3 authors.

Michael GreenacreDepartment of Economics and Business, Universitat Pompeu Fabra, Barcelona, Spain.
Marina Martínez-ÁlvaroDepartment of Agriculture, Horticulture and Engineering Sciences, Scotland's Rural College, Edinburgh, United Kingdom.
Agustín BlascoInstitute for Animal Science and Technology, Universitat Politècnica de València, València, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbiome and omics datasets are, by their intrinsic biological nature, of high dimensionality, characterized by counts of large numbers of components (microbial genes, operational taxonomic units, RNA transcripts, etc.). These data are generally regarded as compositional since the total number of counts identified within a sample is irrelevant. The central concept in compositional data analysis is the logratio transformation, the simplest being the additive logratios with respect to a fixed reference component. A full set of additive logratios is not isometric, that is they do not reproduce the geometry of all pairwise logratios exactly, but their lack of isometry can be measured by the Procrustes correlation. The reference component can be chosen to maximize the Procrustes correlation between the additive logratio geometry and the exact logratio geometry, and for high-dimensional data there are many potential references. As a secondary criterion, minimizing the variance of the reference component's log-transformed relative abundance values makes the subsequent interpretation of the logratios even easier. On each of three high-dimensional omics datasets the additive logratio transformation was performed, using references that were identified according to the abovementioned criteria. For each dataset the compositional data structure was successfully reproduced, that is the additive logratios were very close to being isometric. The Procrustes correlations achieved for these datasets were 0.9991, 0.9974, and 0.9902, respectively. We thus demonstrate, for high-dimensional compositional data, that additive logratios can provide a valid choice as transformed variables, which (a) are subcompositionally coherent, (b) explain 100% of the total logratio variance and (c) come measurably very close to being isometric. The interpretation of additive logratios is much simpler than the complex isometric alternatives and, when the variance of the log-transformed reference is very low, it is even simpler since each additive logratio can be identified with a corresponding compositional component.

Indexed as

compositional datadimension reductionlogratio geometrylogratio transformationlogratio varianceProcrustes correlationvariable selection

Identifiers

PMID34737726
PMCPMC8561721

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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.