I-FLOP: Fast Learning of Order and Parents from Interventional Data

We study fully online fixed-confidence causal discovery without any historical observational data. Starting from zero samples, the learner sequentially selects interventions to recover both the causal DAG and its edge weights under a linear-Gaussian structural equation model. We establish an instance-dependent lower bound for any $(ε,δ)$-correct algorithm and propose FOCUS, which adaptively allocates interventions through an online max--min game. A key contribution is a computable concentration inequality for the accumulated KL divergence involving causal parameters shared across interventions. We prove that FOCUS is $(ε,δ)$-correct and that its expected stopping time matches the lower bound in its $Θ(\log(1/δ))$ dependence up to an instance-dependent constant. Experiments demonstrate improved structure and edge-weight recovery and confirm the predicted stopping-time trend. Our codes are available on https://anonymous.4open.science/r/FOCUS_code-76E5

Graphical approaches to causal abstraction transform a low-level causal directed acyclic graph (DAG) over many measured variables into a smaller, high-level DAG whose nodes cluster the original variables and whose edges summarize the causal relations between clusters. Such cluster DAGs are easier to interpret, but learning them requires finding the clusters and recovering the edges between them. Madaleno et al. (2026) learn the interventional coarsening (the cluster DAG that merges variables the interventions cannot distinguish) in two constraint-based phases: first the clusters, then the edges. We introduce COARSE, the first score-based method for this task: it keeps the two-phase structure but, under linear Gaussian assumptions, swaps the constraint-based edge phase for a score-based one. We show that the interventions themselves identify a causal order over the clusters, and learning the edges reduces to a single local search per cluster under a cluster-level BIC score. We prove that the procedure runs in polynomial time and, provided the variables affected by each intervention are correctly identified, that it is consistent. On synthetic and real-world interventional data, COARSE matches state-of-the-art edge recovery given enough samples, with an edge phase up to two orders of magnitude faster, including on dense graphs with hundreds of nodes.

Learning causal graphs from interventional data is a challenging problem with broad applications. In molecular biology, for example, a central goal is to uncover gene regulatory networks from large-scale perturbation data. An ideal algorithm for this task should scale to thousands of nodes, incorporate interventions even when their targets are unknown, quantify uncertainty, and provide identifiability guarantees. However, existing approaches---e.g. approaches using score-based optimization or approximate Bayesian inference---often fail to meet all of these criteria. To address these limitations, we develop Amortized Bayesian Causal Discovery of Extended Factor Graphs (ABCDEFG). Our method guarantees exact acyclicity, scales to graphs with thousands of nodes, and naturally handles interventions even when their targets are unknown. Additionally, ABCDEFG estimates a posterior distribution whose maximum a posteriori estimate provably identifies the true causal graph up to an equivalence class. On simulated datasets, ABCDEFG achieves state-of-the-art accuracy, producing a well-calibrated posterior distribution while outperforming previous score-based and approximate Bayesian methods. Applied to large-scale single-cell perturbation data, ABCDEFG identifies both established and novel gene targets of growth factors.