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Badri, M.

Publications and source records attributed to Badri, M..

3 recordsLinked to original sources

Moving from Association to Causation: Instrumental factor models for causal inference in high-dimensional multi-omics data

Distinguishing true causal relationships from mere association is a core challenge in bioinformatics and science in general. Causal inference, in particular in "-omics" studies, is hindered by high dimensionality, correlated measurements, and pervasive endogeneity arising from unmeasured confounding and complex interventions. We introduce Factor IV, a supervised instrumental variable (IV) framework for identifying causal effects in high-dimensional biological systems. FactorIV constructs low-dimensional instrumental factors via a sparse low-rank decomposition of the instrument-exposure map, yielding an identifiable first stage even when either/both endogenous and instrumental variables are high-dimensional. Under standard IV assumptions, these factors remain orthogonal to outcome noise while capturing coordinated, perturbation-driven biological variation. The framework supports generalized first-stage models, including Gaussian, Bernoulli and negative binomial likelihoods. Simulation studies demonstrate accurate recovery of factor-level and feature-level causal effects under linear and generalized settings, with robustness to correlated errors and hidden confounding. To illustrate biological discovery, we applied FactorIV to a mouse hepatocellular carcinoma model and the DIABIMMUNE infant cohort. We demonstrate how FactorIV uncovers mechanistically interpretable causal structure beyond association-based analyses.

bioinformatics↗

Revisiting microbe-metabolite interactions: doing better than random

I.Recently, Quinn and Erb et al [1] made the case that when used correctly, correlation and proportionality can outperform MMvec when identifying microbe-metabolite interactions. We revisit this comparison and show that the proposed correlation and proportionality are outperformed by MMvec on real data due to their inability to deal with sparsity commonly observed in microbiome and metabolome datasets.

bioinformatics↗

Normalization methods for microbial abundance data strongly affect correlation estimates

Consistent estimation of associations in microbial genomic survey count data is fundamental to microbiome research. Technical limitations, including compositionality, low sample sizes, and technical variability, obstruct standard application of association measures and require data normalization prior to estimating associations. Here, we investigate the interplay between data normalization and microbial association estimation by a comprehensive analysis of statistical consistency. Leveraging the large sample size of the American Gut Project (AGP), we assess the consistency of the two prominent linear association estimators, correlation and proportionality, under different sample scenarios and data normalization schemes, including RNA-seq analysis work flows and log-ratio transformations. We show that shrinkage estimation, a standard technique in high-dimensional statistics, can universally improve the quality of association estimates for microbiome data. We find that large-scale association patterns in the AGP data can be grouped into five normalization-dependent classes. Using microbial association network construction and clustering as examples of exploratory data analysis, we show that variance-stabilizing and log-ratio approaches provide for the most consistent estimation of taxonomic and structural coherence. Taken together, the findings from our reproducible analysis workflow have important implications for microbiome studies in multiple stages of analysis, particularly when only small sample sizes are available.

bioinformatics↗