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Eric V. Strobl

Publications and source records attributed to Eric V. Strobl.

27 records · Page 2Linked to original sources

Causal Discovery with a Mixture of DAGs

Causal processes in biomedicine may contain cycles, evolve over time or differ between populations. However, many graphical models cannot accommodate these conditions. We propose to model causation using a mixture of directed cyclic graphs (DAGs), where the joint distribution in a population follows a DAG at any single point in time but potentially different DAGs across time. We also introduce an algorithm called Causal Inference over Mixtures that uses longitudinal data to infer a graph summarizing the causal relations generated from a mixture of DAGs. Experiments demonstrate improved performance compared to prior approaches.

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The Global Markov Property for a Mixture of DAGs

Real causal processes may contain feedback loops and change over time. In this paper, we model cycles and non-stationary distributions using a mixture of directed acyclic graphs (DAGs). We then study the conditional independence (CI) relations induced by a density that factorizes according to a mixture of DAGs in two steps. First, we generalize d-separation for a single DAG to mixture d-separation for a mixture of DAGs. We then utilize the mixture d-separation criterion to derive a global Markov property that allows us to read off the CI relations induced by a mixture of DAGs using a particular summary graph. This result has potentially far reaching applications in algorithm design for causal discovery.

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A Constraint-Based Algorithm For Causal Discovery with Cycles, Latent Variables and Selection Bias

Causal processes in nature may contain cycles, and real datasets may violate causal sufficiency as well as contain selection bias. No constraint-based causal discovery algorithm can currently handle cycles, latent variables and selection bias (CLS) simultaneously. I therefore introduce an algorithm called Cyclic Causal Inference (CCI) that makes sound inferences with a conditional independence oracle under CLS, provided that we can represent the cyclic causal process as a non-recursive linear structural equation model with independent errors. Empirical results show that CCI outperforms CCD in the cyclic case as well as rivals FCI and RFCI in the acyclic case.

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Fast Causal Inference with Non-Random Missingness by Test-Wise Deletion

Many real datasets contain values missing not at random (MNAR). In this scenario, investigators often perform list-wise deletion, or delete samples with any missing values, before applying causal discovery algorithms. List-wise deletion is a sound and general strategy when paired with algorithms such as FCI and RFCI, but the deletion procedure also eliminates otherwise good samples that contain only a few missing values. In this report, we show that we can more efficiently utilize the observed values with test-wise deletion while still maintaining algorithmic soundness. Here, test-wise deletion refers to the process of list-wise deleting samples only among the variables required for each conditional independence (CI) test used in constraint-based searches. Test-wise deletion therefore often saves more samples than list-wise deletion for each CI test, especially when we have a sparse underlying graph. Our theoretical results show that test-wise deletion is sound under the justifiable assumption that none of the missingness mechanisms causally affect each other in the underlying causal graph. We also find that FCI and RFCI with test-wise deletion outperform their list-wise deletion and imputation counterparts on average when MNAR holds in both synthetic and real data.

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Estimating and Controlling the False Discovery Rate for the PC Algorithm Using Edge-Specific P-Values

The PC algorithm allows investigators to estimate a complete partially directed acyclic graph (CPDAG) from a finite dataset, but few groups have investigated strategies for estimating and controlling the false discovery rate (FDR) of the edges in the CPDAG. In this paper, we introduce PC with p-values (PC-p), a fast algorithm which robustly computes edge-specific p-values and then estimates and controls the FDR across the edges. PC-p specifically uses the p-values returned by many conditional independence tests to upper bound the p-values of more complex edge-specific hypothesis tests. The algorithm then estimates and controls the FDR using the bounded p-values and the Benjamini-Yekutieli FDR procedure. Modifications to the original PC algorithm also help PC-p accurately compute the upper bounds despite non-zero Type II error rates. Experiments show that PC-p yields more accurate FDR estimation and control across the edges in a variety of CPDAGs compared to alternative methods.

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Approximate Kernel-based Conditional Independence Tests for Fast Non-Parametric Causal Discovery

Constraint-based causal discovery (CCD) algorithms require fast and accurate conditional independence (CI) testing. The Kernel Conditional Independence Test (KCIT) is currently one of the most popular CI tests in the non-parametric setting, but many investigators cannot use KCIT with large datasets because the test scales cubicly with sample size. We therefore devise two relaxations called the Randomized Conditional Independence Test (RCIT) and the Randomized conditional Correlation Test (RCoT) which both approximate KCIT by utilizing random Fourier features. In practice, both of the proposed tests scale linearly with sample size and return accurate p-values much faster than KCIT in the large sample size context. CCD algorithms run with RCIT or RCoT also return graphs at least as accurate as the same algorithms run with KCIT but with large reductions in run time.

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Markov Boundary Discovery with Ridge Regularized Linear Models

Ridge regularized linear models (RRLMs), such as ridge regression and the SVM, are a popular group of methods that are used in conjunction with coefficient hypothesis testing to discover explanatory variables with a significant multivariate association to a response. However, many investigators are reluctant to draw causal interpretations of the selected variables due to the incomplete knowledge of the capabilities of RRLMs in causal inference. Under reasonable assumptions, we show that a modified form of RRLMs can get very close to identifying a subset of the Markov boundary by providing a worst-case bound on the space of possible solutions. The results hold for any convex loss, even when the underlying functional relationship is nonlinear, and the solution is not unique. Our approach combines ideas in Markov boundary and sufficient dimension reduction theory. Experimental results show that the modified RRLMs are competitive against state-of-the-art algorithms in discovering part of the Markov boundary from gene expression data.

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Dependence versus Conditional Dependence in Local Causal Discovery from Gene Expression Data

Motivation: Algorithms that discover variables which are causally related to a target may inform the design of experiments. With observational gene expression data, many methods discover causal variables by measuring each variable's degree of statistical dependence with the target using dependence measures (DMs). However, other methods measure each variable's ability to explain the statistical dependence between the target and the remaining variables in the data using conditional dependence measures (CDMs), since this strategy is guaranteed to find the target's direct causes, direct effects, and direct causes of the direct effects in the infinite sample limit. In this paper, we design a new algorithm in order to systematically compare the relative abilities of DMs and CDMs in discovering causal variables from gene expression data. Results: The proposed algorithm using a CDM is sample efficient, since it consistently outperforms other state-of-the-art local causal discovery algorithms when samples sizes are small. However, the proposed algorithm using a CDM outperforms the proposed algorithm using a DM only when sample sizes are above several hundred. These results suggest that accurate causal discovery from gene expression data using current CDM-based algorithms requires datasets with at least several hundred samples. Availability: The proposed algorithm is freely available at https://github.com/ericstrobl/DvCD.

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Markov Blanket Ranking using Kernel-based Conditional Dependence Measures

Developing feature selection algorithms that move beyond a pure correlational to a more causal analysis of observational data is an important problem in the sciences. Several algorithms attempt to do so by discovering the Markov blanket of a target, but they all contain a forward selection step which variables must pass in order to be included in the conditioning set. As a result, these algorithms may not consider all possible conditional multivariate combinations. We improve on this limitation by proposing a backward elimination method that uses a kernel-based conditional dependence measure to identify the Markov blanket in a fully multivariate fashion. The algorithm is easy to implement and compares favorably to other methods on synthetic and real datasets.

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