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Coler, E. A.

Publications and source records attributed to Coler, E. A..

2 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↗

Ordering molecular diversity in untargeted metabolomics via molecular community networking

Natures molecular diversity is not random but displays intricate organization stemming from biological necessity. Molecular networking connects metabolites with structural similarity, enabling molecular discoveries from mass spectrometry data using arbitrary similarity thresholds that can fracture natural metabolite families. We present molecular community networking (MCN), that optimizes connectivity for each metabolite, rescuing lost relationships and capturing otherwise "hidden" metabolite connections. Using MCN, we demonstrate the discovery of novel dipeptide-conjugated bile acids.

biochemistry↗