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Susin, A.

Publications and source records attributed to Susin, A..

3 recordsLinked to original sources

Understanding the bias of compositional microbiome differential abundance estimation

One of the most relevant objectives in microbiome studies is the identification of microbial species that are differentially abundant across conditions. However, the compositional nature of microbiome data complicates this task. Interdependence among components leads to spurious associations when the abundances of each component are analyzed separately. Due to the growing awareness of the challenges of compositional data analysis (CoDA), log-ratio transformations, such as the additive log-ratio (alr) or the centered log-ratio (clr) transformations, have become increasingly popular in microbiome studies. Several studies have compared the performance of compositional and non-compositional methods through simulations. However, the debate between these two frameworks remains unresolved, creating confusion among researchers. Rather than relying on simulation-based results, this work provides theoretical results that enable a more rigorous and conclusive analysis of the problem, contributing to a better understanding of differential abundance estimation. We provide theoretical expressions of the bias of differential abundance estimation related to the use of proportions (total sum scaling) and log-ratio transformations (alr and clr) when estimates are interpreted as absolute rather than relative to a reference. The factors that most strongly influence the bias are the magnitude and direction of the effects, the dimension of the composition, the proportion of differentially abundant variables, and the distribution of relative abundances. The findings of this work strongly support the use of CoDA transformations; however, they also highlight that even when log-ratio transformations are applied, interpreting the results outside of a CoDA framework can still lead to biased conclusions. Among CoDA transformations, alr has several advantages over clr: its reference is more explicit, which reduces the risk of interpreting estimates as absolute rather than relative, and it facilitates the replication of results in independent studies, as it only requires assessing changes relative to the same reference rather than reconstructing the full composition. In this work, we propose a heuristic method for selecting a suitable alr reference component, which will enable a more widespread use of this transformation.

bioinformatics↗

coda4microbiome: compositional data analysis for microbiome studies

MotivationOne of the main challenges of microbiome analysis is its compositional nature that if ig-nored can lead to spurious results. This is especially critical when dealing with microbiome variable selection since classical differential abundance tests are known to provide large false positive rates. ResultsWe developed coda4microbiome, a new R package for analyzing microbiome data within the Compositional Data Analysis (CoDA) framework in both, cross-sectional and longitudinal studies. The core functions of the library are aimed at the identification of microbial signatures and involve variable selection in generalized linear models with compositional covariates. All algorithms are accompanied by meaningful graphical representations that allow a better interpretation of the results. Availabilitycoda4microbiome is implemented as an R package and is available at CRAN https://cran.r-project.org/web/packages/coda4microbiome/index.html. Contactmalu.calle@uvic.cat Supplementary informationcoda4microbiome project website: https://malucalle.github.io/coda4mi-crobiome/.

microbiology↗

IDENTIFICATION OF DYNAMIC MICROBIAL SIGNATURES IN LONGITUDINAL STUDIES

The study of microbiome dynamics is key for unveiling the role of the microbiome in human health. Addressing the compositional structure of microbiome data is particularly critical in longitudinal studies where compositions measured at different times can yield to different subcompositions. We propose a new compositional data analysis (CoDA) algorithm for inferring dynamic microbial signatures. The algorithm performs penalized regression over the summary of the log-ratio trajectories (the area under these trajectories) and the inferred microbial signature is expressed as a log-contrast model. Graphical representations of the results are provided to facilitate the interpretation of the analysis: plot of the log-ratio trajectories, plot of the signature and plot of the prediction accuracy of the model. The new proposal is illustrated with data on the developing microbiome of infants. The algorithm is implemented in the R package "code4microbiome" (https://cran.r-project.org/web/packages/coda4microbiome/) that is accompanied with a vignette with a detailed description of the functions. The website of the project contains several tutorials: https://malucalle.github.io/coda4microbiome/

bioinformatics↗