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Causal Discovery with Generalized Linear Models through Peeling Algorithms

2023/10/25 by Minjie Wang, Wang, Minjie, Xiaotong Shen +3
Computer Science · #Bayesian Modeling and Causal Inference #FOS: Computer and information sciences #Machine Learning (stat.ML) #Machine Learning and Data Classification #Methodology (stat.ME) #Rough Sets and Fuzzy Logic

paper · doi:10.48550/arxiv.2310.16698

openalex publication_date 2023/10/25 · openalex created_date 2023/10/27 · openalex updated_date 2026/08/01

Abstract

This article presents a novel method for causal discovery with generalized structural equation models suited for analyzing diverse types of outcomes, including discrete, continuous, and mixed data. Causal discovery often faces challenges due to unmeasured confounders that hinder the identification of causal relationships. The proposed approach addresses this issue by developing two peeling algorithms (bottom-up and top-down) to ascertain causal relationships and valid instruments. This approach first reconstructs a super-graph to represent ancestral relationships between variables, using a peeling algorithm based on nodewise GLM regressions that exploit relationships between primary and instrumental variables. Then, it estimates parent-child effects from the ancestral relationships using another peeling algorithm while deconfounding a child's model with information borrowed from its parents' models. The article offers a theoretical analysis of the proposed approach, establishing conditions for model identifiability and providing statistical guarantees for accurately discovering parent-child relationships via the peeling algorithms. Furthermore, the article presents numerical experiments showcasing the effectiveness of our approach in comparison to state-of-the-art structure learning methods without confounders. Lastly, it demonstrates an application to Alzheimer's disease (AD), highlighting the method's utility in constructing gene-to-gene and gene-to-disease regulatory networks involving Single Nucleotide Polymorphisms (SNPs) for healthy and AD subjects.

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