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Causal Discovery with Generalized Linear Models through Peeling Algorithms.

Minjie Wang1, Xiaotong Shen2, Wei Pan3

  • 1Department of Mathematics and Statistics, Binghamton University, State University of New York, Binghamton, NY 13902, USA.

Journal of Machine Learning Research : JMLR
|January 6, 2025
PubMed
Summary
This summary is machine-generated.

This study introduces a new causal discovery method using generalized structural equation models to identify relationships even with unmeasured confounders. The novel peeling algorithms accurately uncover causal links and apply to complex data, including Alzheimer's disease genetics.

Keywords:
Generalized linear modelshierarchylarge directed acyclic graphsmixed graphical modelsnonconvex minimization

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Area of Science:

  • Causal inference
  • Statistical genetics
  • Machine learning

Background:

  • Causal discovery is challenged by unmeasured confounders, complicating relationship identification.
  • Generalized structural equation models (GSEMs) offer flexibility for diverse data types but require robust causal discovery methods.
  • Existing methods often struggle with unmeasured confounding and mixed data outcomes.

Purpose of the Study:

  • To develop a novel causal discovery method for GSEMs applicable to discrete, continuous, and mixed data.
  • To address the challenge of unmeasured confounders in identifying causal relationships.
  • To provide a robust framework for constructing gene regulatory networks.

Main Methods:

  • Developed two peeling algorithms (bottom-up and top-down) for causal discovery and instrument identification.
  • Reconstructed a super-graph of ancestral relationships using nodewise GLM regressions.
  • Estimated parent-child effects by deconfounding child models with parent information.

Main Results:

  • Established theoretical conditions for model identifiability and statistical guarantees for discovering parent-child relationships.
  • Numerical experiments demonstrated superior performance compared to state-of-the-art methods.
  • Successfully applied the method to construct gene-to-gene and gene-to-disease networks in Alzheimer's disease using SNPs.

Conclusions:

  • The proposed peeling algorithms effectively perform causal discovery in the presence of unmeasured confounders.
  • The method is robust for analyzing diverse data types within GSEMs.
  • Demonstrated practical utility in unraveling complex biological networks, such as those in Alzheimer's disease.