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. IMPORTANCE High-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.
Hoseung Song, Yunhua Xiang, Hongjiao Liu et al.· bioRxiv· 0 citations
Previous association studies between germline rare genetic variation and cancer risk have primarily examined a limited number of cancers in clinical samples, often with participants predominantly of European genetic ancestry. We conducted exome-wide rare variant association analyses across 70+ cancer types using data from more than 729,000 participants from the UK Biobank (UKB) and All of Us Research Program (AoU) cohorts. We used generalized linear mixed models to screen for cancer pleiotropic effects by conducting gene-based and single variant tests of predicted loss of function (pLoF) and missense variants and six groups of cancer defined by biological and etiological similarities. We then assessed significant genes for associations with 27 individual cancer types that had data for at least 500 cases. Of the 33 potential pleiotropic genes identified, 16 consistently showed significant associations across ≥ 3 individual cancer types. For example, the presence of at least one CHEK2 pLoF variant was associated with increased odds of diagnosis with 14 different cancers (OR range: 1.34 - 3.21). Similarly, the presence of at least one RTEL1 missense variant was associated with lower odds of diagnosis with 9 cancers (OR range: 0.67 - 0.88). Our results expand our knowledge about these loci and point to a larger impact on overall cancer risk than previously appreciated.
A. H. Suger, T. Harrison, Jiachen Zhang et al.· HGG advances· 0 citations
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