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Plantinga, A. M.

Publications and source records attributed to Plantinga, A. M..

3 recordsLinked to original sources

Constructing microbiome co-occurrence networks with confidence: A conditional, nonparametric, inference-based approach

Constructing microbial association networks is a common strategy for exploring relationships among taxa in microbiome studies. Although marginal correlation methods are easy to implement and allow formal inference, they can produce spurious edges driven by indirect associations through other taxa. Conditional graphical-modeling methods aim to recover direct associations, but many rely on Gaussian or linear assumptions and often provide limited uncertainty quantification. We propose a conditional, nonparametric approach based on the scaled expected conditional covariance (SEcov). SEcov measures population-level conditional association by residualizing each taxon with respect to the remaining taxa and scaling the resulting expected conditional covariance. The resulting estimator can incorporate flexible machine-learning methods for conditional-mean estimation and admits asymptotic normal inference, enabling p-values and confidence intervals for taxon-pair associations. We demonstrate through simulation studies that our proposed approach improves network recovery relative to other methods, and we illustrate the new method via construction of a co-occurrence network for the vaginal microbiome during pregnancy. IMPORTANCEHigh-throughput sequencing has made it possible to characterize microbial communities at large scale, and network analysis is widely used to summarize relationships among taxa. However, networks based on marginal correlations may include indirect associations, whereas many conditional graphical models rely on assumptions that may be difficult to justify for sparse, zero-inflated, compositional microbiome data. SEcov offers a practical alternative by estimating conditional associations nonparametrically and attaching inferential uncertainty to individual edges. This allows investigators to construct microbiome networks using statistically interpretable evidence for taxon-pair associations, rather than relying solely on arbitrary correlation cutoffs or regularization tuning parameters.

bioinformatics↗

Kernel-based genetic association analysis for microbiome phenotypes identifies host genetic drivers of beta-diversity

Understanding human genetic influences on the gut microbiota helps elucidate the mechanisms by which genetics affects health outcomes. We propose a novel approach, the covariate-adjusted kernel RV (KRV) framework, to map genetic variants associated with microbiome beta-diversity, which focuses on overall shifts in the microbiota. The proposed KRV framework improves statistical power by capturing intrinsic structure within the genetic and microbiome data while reducing the multiple-testing burden. We apply the covariate-adjusted KRV test to the Hispanic Community Health Study/Study of Latinos in a genome-wide association analysis (first gene-level, then variant-level) for microbiome beta-diversity. We have identified an immunity-related gene, IL23R, reported in previous association studies and discovered 3 other novel genes, 2 of which are involved in immune functions or autoimmune disorders. Our findings highlight the value of the KRV as a powerful microbiome GWAS approach and support an important role of immunity-related genes in shaping the gut microbiome composition.

genomics↗

Batch effects removal for microbiome data via conditional quantile regression (ConQuR)

Batch effects in microbiome data arise from differential processing of specimens and can lead to spurious findings and obscure true signals. Most existing strategies for mitigating batch effects rely on approaches designed for genomic analysis, failing to address the zero-inflated and over-dispersed microbiome data. Strategies tailored for microbiome data are restricted to association testing, failing to allow other analytic goals such as visualization. We develop the Conditional Quantile Regression (ConQuR) approach to remove microbiome batch effects using a two-part quantile regression model. It is a fundamental advancement in the field because it is the first comprehensive method that accommodates the complex distributions of microbial read counts, and it generates batch-removed zero-inflated read counts that can be used in and benefit all usual subsequent analyses. We apply ConQuR to real microbiome data sets and demonstrate its state-of-the-art performance in removing batch effects while preserving or even amplifying the signals of interest.

bioinformatics↗