Root cause discovery via permutations and Cholesky decomposition

Abstract This work is motivated by the following problem: Can we identify the disease-causing gene in a patient affected by a monogenic disorder? This problem is an instance of root cause discovery. Specifically, we aim to identify the intervened variable in one interventional sample using a set of observational samples as reference. We consider a linear structural equation model where the causal ordering is unknown. We begin by examining a simple method that uses squared z-scores and characterize the conditions under which this method succeeds and fails, showing it generally cannot identify the root cause. We then prove, without additional assumptions, that the root cause is identifiable even if the causal ordering is not. Two key ingredients of this identifiability result are the use of permutations and the Cholesky decomposition, which allow us to exploit an invariant property across different permutations to discover the root cause. Furthermore, we characterize permutations that yield the correct root cause and, based on this, propose a valid method for root cause discovery. We also adapt this approach to high-dimensional settings. Finally, we evaluate our methods through simulations and apply the high-dimensional method to discover disease-causing genes in the gene expression dataset that motivates this work.

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Publication Details

Journal
Journal of the Royal Statistical Society Series B (Statistical Methodology)
Published
2025-10-16
DOI
https://doi.org/10.1093/jrsssb/qkaf066
Primary Topic
DNA and Biological Computing
Type
article
Field-Weighted Citation Impact
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article

Root cause discovery via permutations and Cholesky decomposition

Julien Gagneur, Benjamin B. Chu, Marloes H. Maathuis, Ines F. Scheller et al.
Journal of the Royal Statistical Society Series B (Statistical Methodology)
DNA and Biological Computing
article

Root cause discovery via permutations and Cholesky decomposition

Julien Gagneur, Benjamin B. Chu, Marloes H. Maathuis, Ines F. Scheller, Jinzhou Li
article en

Abstract

Abstract This work is motivated by the following problem: Can we identify the disease-causing gene in a patient affected by a monogenic disorder? This problem is an instance of root cause discovery. Specifically, we aim to identify the intervened variable in one interventional sample using a set of observational samples as reference. We consider a linear structural equation model where the causal ordering is unknown. We begin by examining a simple method that uses squared z-scores and characterize the conditions under which this method succeeds and fails, showing it generally cannot identify the root cause. We then prove, without additional assumptions, that the root cause is identifiable even if the causal ordering is not. Two key ingredients of this identifiability result are the use of permutations and the Cholesky decomposition, which allow us to exploit an invariant property across different permutations to discover the root cause. Furthermore, we characterize permutations that yield the correct root cause and, based on this, propose a valid method for root cause discovery. We also adapt this approach to high-dimensional settings. Finally, we evaluate our methods through simulations and apply the high-dimensional method to discover disease-causing genes in the gene expression dataset that motivates this work.

Journal of the Royal Statistical Society Series B (Statistical Methodology)
National University of Singapore (SG), Helmholtz Zentrum München (DE), ETH Zurich (CH), Institute of Human Genetics (PL), Technical University of Munich (DE), Stanford University (US)
Openalex Percentile: Top 74%
DNA and Biological Computing
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