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Benchmarking microbiome transformations favors experimental quantitative approaches to address compositionality and sampling depth biases

Author

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  • Verónica Lloréns-Rico

    (Rega Institute, KU Leuven
    Center for Microbiology, VIB)

  • Sara Vieira-Silva

    (Rega Institute, KU Leuven
    Center for Microbiology, VIB)

  • Pedro J. Gonçalves

    (Center of Advanced European Studies and Research (caesar))

  • Gwen Falony

    (Rega Institute, KU Leuven
    Center for Microbiology, VIB)

  • Jeroen Raes

    (Rega Institute, KU Leuven
    Center for Microbiology, VIB)

Abstract

While metagenomic sequencing has become the tool of preference to study host-associated microbial communities, downstream analyses and clinical interpretation of microbiome data remains challenging due to the sparsity and compositionality of sequence matrices. Here, we evaluate both computational and experimental approaches proposed to mitigate the impact of these outstanding issues. Generating fecal metagenomes drawn from simulated microbial communities, we benchmark the performance of thirteen commonly used analytical approaches in terms of diversity estimation, identification of taxon-taxon associations, and assessment of taxon-metadata correlations under the challenge of varying microbial ecosystem loads. We find quantitative approaches including experimental procedures to incorporate microbial load variation in downstream analyses to perform significantly better than computational strategies designed to mitigate data compositionality and sparsity, not only improving the identification of true positive associations, but also reducing false positive detection. When analyzing simulated scenarios of low microbial load dysbiosis as observed in inflammatory pathologies, quantitative methods correcting for sampling depth show higher precision compared to uncorrected scaling. Overall, our findings advocate for a wider adoption of experimental quantitative approaches in microbiome research, yet also suggest preferred transformations for specific cases where determination of microbial load of samples is not feasible.

Suggested Citation

  • Verónica Lloréns-Rico & Sara Vieira-Silva & Pedro J. Gonçalves & Gwen Falony & Jeroen Raes, 2021. "Benchmarking microbiome transformations favors experimental quantitative approaches to address compositionality and sampling depth biases," Nature Communications, Nature, vol. 12(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23821-6
    DOI: 10.1038/s41467-021-23821-6
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    Cited by:

    1. Ben O. Oyserman & Stalin Sarango Flores & Thom Griffioen & Xinya Pan & Elmar Wijk & Lotte Pronk & Wouter Lokhorst & Azkia Nurfikari & Joseph N. Paulson & Mercedeh Movassagh & Nejc Stopnisek & Anne Kup, 2022. "Disentangling the genetic basis of rhizosphere microbiome assembly in tomato," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
    2. Oliver Aasmets & Kertu Liis Krigul & Kreete Lüll & Andres Metspalu & Elin Org, 2022. "Gut metagenome associations with extensive digital health data in a volunteer-based Estonian microbiome cohort," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    3. Alice Risely & Kerstin Wilhelm & Tim Clutton-Brock & Marta B. Manser & Simone Sommer, 2021. "Diurnal oscillations in gut bacterial load and composition eclipse seasonal and lifetime dynamics in wild meerkats," Nature Communications, Nature, vol. 12(1), pages 1-12, December.

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