interventional distribution
DeCaFlow: A deconfounding causal generative model
We introduce DeCaFlow, a deconfounding causal generative model. Training once per dataset using just observational data and the underlying causal graph, DeCaFlow enables accurate causal inference on continuous variables under the presence of hidden confounders. Specifically, we extend previous results on causal estimation under hidden confounding to show that a single instance of DeCaFlow provides correct estimates for all causal queries identifiable with do-calculus, leveraging proxy variables to adjust for the causal effects when do-calculus alone is insufficient. Moreover, we show that counterfactual queries are identifiable as long as their interventional counterparts are identifiable, and thus are also correctly estimated by DeCaFlow. Our empirical results on diverse settings--including the Ecoli70 dataset, with 3 independent hidden confounders, tens of observed variables and hundreds of causal queries--show that DeCaFlow outperforms existing approaches, while demonstrating its out-of-the-box applicability to any given causal graph.
Characterization and Learning of Causal Graphs from Hard Interventions
A fundamental challenge in the empirical sciences involves uncovering causal structure through observation and experimentation. Causal discovery entails linking the conditional independence (CI) invariances in observational data to their corresponding graphical constraints via d-separation. In this paper, we consider a general setting where we have access to data from multiple experimental distributions resulting from hard interventions, as well as potentially from an observational distribution. By comparing different interventional distributions, we propose a set of graphical constraints that are fundamentally linked to Pearl's do-calculus within the framework of hard interventions. These graphical constraints associate each graphical structure with a set of interventional distributions that are consistent with the rules of do-calculus. We characterize the interventional equivalence class of causal graphs with latent variables and introduce a graphical representation that can be used to determine whether two causal graphs are interventionally equivalent, i.e., whether they are associated with the same family of hard interventional distributions, where the elements of the family are indistinguishable using the invariances from do-calculus. We also propose a learning algorithm to integrate multiple datasets from hard interventions, introducing new orientation rules. The learning objective is a tuple of augmented graphs which entails a set of causal graphs. We also prove the soundness of the proposed algorithm.
Characterization and Learning of Causal Graphs from Hard Interventions
A fundamental challenge in the empirical sciences involves uncovering causal structure through observation and experimentation. Causal discovery entails linking the conditional independence (CI) invariances in observational data to their corresponding graphical constraints via d-separation. In this paper, we consider a general setting where we have access to data from multiple experimental distributions resulting from hard interventions, as well as potentially from an observational distribution. By comparing different interventional distributions, we propose a set of graphical constraints that are fundamentally linked to Pearl's do-calculus within the framework of hard interventions. These graphical constraints associate each graphical structure with a set of interventional distributions that are consistent with the rules of do-calculus. We characterize the interventional equivalence class of causal graphs with latent variables and introduce a graphical representation that can be used to determine whether two causal graphs are interventionally equivalent, i.e., whether they are associated with the same family of hard interventional distributions, where the elements of the family are indistinguishable using the invariances from do-calculus. We also propose a learning algorithm to integrate multiple datasets from hard interventions, introducing new orientation rules. The learning objective is a tuple of augmented graphs which entails a set of causal graphs. We also prove the soundness of the proposed algorithm.
Extended Wasserstein-GAN Approach to Causal Distribution Learning: Density-Free Estimation and Minimax Optimality
Tamano, Shu, Imaizumi, Masaaki
Distributional causal inference requires estimating not only average treatment effects but also interventional outcome distributions, including quantiles, tail risks, and policy-dependent uncertainty. As a method for distributional causal inference, generative adversarial network (GAN)-based counterfactual methods are flexible tools for this task. However, these methods have several limitations. First, the objectives of certain techniques do not coincide with the statistical risk of the identifiable causal target, and therefore provide limited theoretical guarantees regarding estimable counterfactual distributions or optimality. Second, they tend to rely on unstable density-based methods, such as density ratio estimation. In this paper, we propose GANICE (GAN for Interventional Conditional Estimation) with several advantages: it (i) clarifies the conditional interventional distribution for each treatment--covariate state as the causal estimation target; (ii) estimates the conditional distribution such that its averaged Wasserstein risk is minimized; (iii) establishes minimax optimality. GANICE achieves these advantages through the introduction of the extended Wasserstein distance, the incorporation of a cellwise critic in its dual, and an optimality proof based on Besov space theory. Our experiments demonstrate that GANICE consistently outperforms existing methods.
TabCF: Distributional Control Function Estimation with Tabular Foundation Models
Chen, Geping, Li, Chunlin, Yang, Tianzhong, Zhu, Zhengyuan, Zhou, Jing
Instrumental variable (IV) and control function (CF) methods are powerful tools for causal effect estimation in the presence of unmeasured confounding, yet most existing approaches target only mean effects and/or demand substantial fitting and tuning effort. In this paper, we introduce a simple method, TabCF, for control function regression using tabular foundation models, which enables accurate, fast, identification-transparent, and tuning-light causal estimation of distributional quantities, such as interventional means and quantiles; we also propose a copula-based approximation for multivariate outcomes. TabCF performs favorably against representative methods across a broad range of small- to medium-sized synthetic and real data scenarios. The central message is two-fold: for practitioners, it highlights that TabCF is an effective tool for distributional causal inference; for researchers, it suggests that the proposed approach could be considered a strong baseline for future method development. Code is available at https://github.com/GepingChen/TabCF.
Conditional Generative Models are Sufficient to Sample from Any Causal Effect Estimand
Causal inference from observational data plays critical role in many applications in trustworthy machine learning.While sound and complete algorithms exist to compute causal effects, many of them assume access to conditional likelihoods, which is difficult to estimate for high-dimensional (particularly image) data. Researchers have alleviated this issue by simulating causal relations with neural models. However, when we have high-dimensional variables in the causal graph along with some unobserved confounders, no existing work can effectively sample from the un/conditional interventional distributions. In this work, we show how to sample from any identifiable interventional distribution given an arbitrary causal graph through a sequence of push-forward computations of conditional generative models, such as diffusion models. Our proposed algorithm follows the recursive steps of the existing likelihood-based identification algorithms to train a set of feed-forward models, and connect them in a specific way to sample from the desired distribution. We conduct experiments on a Colored MNIST dataset having both the treatment ($X$) and the target variables ($Y$) as images and sample from $P(y|do(x))$. Our algorithm also enables us to conduct a causal analysis to evaluate spurious correlations among input features of generative models pre-trained on the CelebA dataset. Finally, we generate high-dimensional interventional samples from the MIMIC-CXR dataset involving text and image variables.
Learning Mixtures of Unknown Causal Interventions
The ability to conduct interventions plays a pivotal role in learning causal relationships among variables, thus facilitating applications across diverse scientific disciplines such as genomics, economics, and machine learning. However, in many instances within these applications, the process of generating interventional data is subject to noise: rather than data being sampled directly from the intended interventional distribution, interventions often yield data sampled from a blend of both intended and unintended interventional distributions.We consider the fundamental challenge of disentangling mixed interventional and observational data within linear Structural Equation Models (SEMs) with Gaussian additive noise without the knowledge of the true causal graph. We demonstrate that conducting interventions, whether do or soft, yields distributions with sufficient diversity and properties conducive to efficiently recovering each component within the mixture. Furthermore, we establish that the sample complexity required to disentangle mixed data inversely correlates with the extent of change induced by an intervention in the equations governing the affected variable values. As a result, the causal graph can be identified up to its interventional Markov Equivalence Class, similar to scenarios where no noise influences the generation of interventional data. We further support our theoretical findings by conducting simulations wherein we perform causal discovery from such mixed data.