Pablo Torrijos, Fabio Stella, José A. Gámez +1cs.LG
In this paper we study linear non-Gaussian acyclic models (LiNGAM) when used in federated environments. These causal models allow one to go beyond Markov equivalence. However, in many domains data are scarce, and increasing the sample size by centralising data from different clients is not advisable due to regulations such as the GDPR. The federated environment offers an attractive option to balance privacy and causal discovery accuracy. Unfortunately, the standard centralised estimator in the LiNGAM setting, i.e., DirectLiNGAM, cannot be straightforwardly federated. Higher-order cumulant tensors offer a way around this obstacle: they depend only on the joint distribution of the variables involved and add exactly across independent sample groups, so a single communication round suffices in horizontal, vertical, and hybrid partitions. However, FedISHC, i.e., the current federated method along these lines, breaks down under near-symmetric noise. To overcome the above limitation, we introduce the FedRCD family of causal discovery algorithms, and investigate three variants that trade off communication rounds against algebraic noise; two of them are exact federated counterparts of the centralised high-order cumulant (HC) and HC-LiNGAM algorithms, and the single-round variants further effectively support exact unlearning at any granularity, from a single observation to a whole client. Numerical experiments show that at sample sizes typical of real deployments, the entire cumulant-based federated family does not actually rank variables by the population asymmetry that the scores encode at zero. It ranks them by a variance ladder induced by the DAG along its directed paths, the cumulant counterpart of varsortability. Marginal standardisation collapses every cumulant method to near-random ordering, while scale-invariant DirectLiNGAM, not federable under this protocol, is unaffected.
Sairam Sundararaman, Sara Girdhar, Manit Narasimha Murthy +2cs.LG
Differentiable causal discovery methods increasingly encode expert priors as forbidden-edge constraints enforced by an Augmented Lagrangian (ALM) penalty, on the assumption that a data-adaptive relaxation mechanism will discount and eventually override a rule the data consistently contradicts. We show this design, which we call \emph{guide, not bind}, fails for two independent, precisely characterized reasons, and that directly repairing both restores it only partially. First, sequential penalty-ramping ALM suppresses a wrongly-forbidden true edge before any counterfactual check can detect it: we give three necessary conditions any adaptive relaxation must satisfy to avoid this (Proposition~\ref{prop:conditions}), prove that DADU---the natural relaxation rule this paper introduces as the object of study---violates all three (Corollary~\ref{cor:dadu_failure}), and confirm the failure across 3{,}072 training runs spanning graphs from 4 to 32 nodes, where a single wrong prior suppresses a true edge in 87--97\% of trials under DADU. Second, and independent of any fix to the mechanism, we prove in closed form that the standard correlation-matching objective ties a true edge and its reverse to an identical cost of exactly $2r^2$ (Lemma~\ref{lem:tie}), not because the underlying equal-variance model is unidentifiable, but because normalizing to correlation discards exactly the variance information that would make it identifiable; covariance matching instead separates the two directions by a provable margin of at least $w_0^4$ (Lemma~\ref{lem:separation}).
TRACE (Math & Lienhart, arXiv:2602.01135) reads causal graphs over event types out of a pretrained autoregressive sequence model by thresholding a per-position conditional-mutual-information estimate at a fixed tau. We independently replicate its headline synthetic result: with tau selected on a validation split, mean per-sequence F1 against exact interventional truth reaches 0.90-0.91 at vocabulary size 1000 (paper: 0.91) and 0.86-0.91 from 100 to 2000. First, the optimal threshold is pinned to the truth margin, not to any constant: at every size the errors at tau* straddle the delta = 0.05 margin defining ground truth (missed true edges lie just above it, accepted false ones just below), and the blind optimum lands near delta/2 times the estimator's calibration, confirmed out of sample at 5000. Second, at a single global threshold TRACE mostly recovers a direct, adjacent-influence graph: lag-1 true edges are recalled at 0.97-0.99, while true edges at lag 2 or more read orders of magnitude lower---the reading-scale price of randomizing mediating positions, which an exact test of direct causal effect requires when the truth is unknown. A per-lag threshold family recovers a third to a half of lag-2 truth; on lag-uniform data one validated threshold recalls every lag at 0.40-0.87, 8-26 pp below an atomic-intervention control at lags 3-6. Third, the default lag decay of the paper's synthetic benchmark concentrates about 85% of interventional truth at lag 1 and pushes the rest below the estimator's noise floor, so headline F1 there certifies lag-1 recovery only and conflates the benchmark's skew with the algorithm's own limit; a flatter decay separates the two. Fourth, F1 saturates from N = 2 particles at the selected threshold---a property of the threshold's margin over the noise floor, not of the estimator, which converges as N^(-1/2). We distill five practitioner rules.
We extend the FLOP (fast learning of order and parents) algorithm recently proposed by Wienöbst et al. (2026) from observational to interventional data. In particular, we use the interventional BIC score of Hauser and Bühlmann (2012), adapting it to be used with the iterative Cholesky-based score updates that are partly responsible for FLOP's speed. We show that, in the sample limit, I-FLOP recovers a DAG in the same interventional Markov equivalence class as the data-generating DAG. We compare I-FLOP to existing causal structure learning algorithms on real and simulated interventional data, where it performs favorably in terms of both performance and run time.
Amit Kumar, Elnur Adl Zarabi, Suranjana Trivedy +4cs.LG cs.AI stat.ME
Large language models (LLMs) are increasingly used to provide prior causal knowledge for structural causal discovery, yet whether their direct-edge judgments and confidence can be trusted remains unclear. We systematically evaluate 12 instruction-tuned open-weight models across six benchmark causal graphs, five prompting strategies, and four confidence sources: verbalized, logit-based, cross-prompt agreement, and cross-model agreement. Under our language-only pairwise protocol, our evaluation yields three key findings. (i) LLM-based causal judgments are strongly recall-dominant: models predict overly dense graphs with many false-positive edges, while prompting mainly shifts the precision-recall trade-off rather than resolving overprediction. Gains from model scale diminish on the largest graphs and do not eliminate miscalibration. (ii) LLMs often capture causal relatedness without reliably identifying directness or orientation. Relative to published reference graphs, models misclassify 40.0% of indirect and 36.0% of reversed non-edges as direct edges, versus 28.2% of other non-edges. Moreover, 80.8% and 84.6% of these false positives receive verbalized confidence of at least 80%, revealing substantial overconfidence in structurally incorrect predictions. (iii) Conventional confidence estimates are unreliable, whereas agreement offers a more promising signal. Logit-based confidence frequently collapses near 1.0 regardless of correctness, while cross-prompt and cross-model agreement achieve better mean calibration and discrimination, though their advantages are not statistically significant after Holm correction. A benchmark-familiarity audit further identifies potential familiarity in five model-dataset pairs, all involving AsiaM. Overall, our results suggest LLMs are better viewed as sources of externally validated soft causal priors than as direct evidence of causal structure.
Causal discovery aims to understand the relationships between individual random variables. In many applications, such as brain imaging and climate modeling, it is more meaningful to consider interactions among groups of variables. Existing methods assume that knowledge of such groups or clusters is explicitly available when modeling interactions. However, in practice, these clusters as well as the causal relationships among them, are latent. In this paper, we present a novel approach based on variational inference to simultaneously infer both the latent clusters and causal structures. We learn an approximate posterior over clusters and graph-structure by considering variational distributions based on categorical and Bernoulli models respectively. We derive variational lower bounds and estimation techniques to learn variational and model parameters. The effectiveness of our proposed methods for cluster and causal discovery are demonstrated on both synthetic and real data sets.
Causal discovery on topological event sequences is crucial for ensuring the reliability of networks. However, existing methods struggle to capture the complex causal relationships arising from concurrent events and lack robustness to incomplete event sequences. To address these issues, we propose a resilient concurrent causal discovery method, termed RCCD, enabling robust learning of causal graphs from topological event sequences. Specifically, we first introduce an influence-aware hyperedge causal attention mechanism, which incorporates event duration into the embedding representation, aggregates concurrent event features via hyperedge causal convolution, and injects network prior knowledge to capture the complex many-to-one causal interactions. Furthermore, we design a masked-based alternating causal optimization framework, which forces the model to recover masked event types based on context through self-supervised mask reconstruction, thereby enhancing the resilience of the predictor to missing data. To validate the effectiveness of our method, we conduct extensive experiments on both simulated and real-world telecommunication network datasets. Experimental results demonstrate that the proposed method significantly outperforms existing state-of-the-art methods in both accuracy and robustness, making it more suitable for real-world telecommunication network environments.
Root cause analysis aims to identify the mechanisms responsible for anomalies in complex dynamical systems. In this paper, we study root cause analysis in linear time-series through the lens of difference graph discovery. We focus on effect-defying root causes, corresponding to variables whose causal coefficients change between a normal and an anomalous regime. We formalize this problem using linear discrete-time dynamic structural causal models and adapt several methods originally introduced for discovering difference graphs between two populations to the time-series setting, where the two populations are replaced by a normal and an anomalous regime. We first evaluate the proposed approaches on simulated data, and then demonstrate their practical relevance on real-world datasets from IT monitoring and intensive care monitoring. Our results show how difference graph discovery can help localize causal mechanisms responsible for anomalous behavior.
Kavimayil P. Komarasamy, Saurabh Mathur, Ameet Soni +3cs.LG
Adverse Pregnancy Outcomes (APOs) such as preterm birth and gestational diabetes can have long-term consequences for both the mother and child, yet an understanding of their causes remains elusive. Causal discovery in this domain is especially challenging due to a paucity of data and incomplete domain knowledge. As a result, pure data-driven methods fail, and Large Language Model (LLM) outputs remain inconsistent or contradictory. We introduce a neurosymbolic framework for generating plausible causal hypotheses that iteratively combines the broad prior knowledge of LLMs with empirical scoring on data. Our method treats the LLM as an adaptive proposal distribution, generating hypotheses that are scored against empirical data; the resulting high-scoring graphs are then used to update the LLM's context, steering subsequent generations toward more promising regions of the hypothesis space. We evaluate our approach on a real-world clinical dataset for modeling APOs and their risk factors, comparing our results against an expert-constructed causal graph. Our method recovers all expert-validated edges and identifies additional plausible causal relations not previously listed by experts, potentially providing new insights for targeted interventions.
The causal dynamics of sleep-disordered breathing are complex and vary across patient populations, hindering the development of targeted interventions. We learn dynamic causal graphs of sleep-disordered breathing from Home Sleep Apnea Test (HSAT) recordings, revealing systematic differences in causal structure across sex and age subcohorts. We do so using the PCMCI+ algorithm on windowed fractional variables derived from 105 HSAT recordings, exploiting domain knowledge via edge blacklisting and employing bootstrap aggregation to address small subcohort sizes. The learned graphs show that temporal self-dependencies and the apnea-desaturation relationship persist across all cohorts, while other relationships vary substantially.
Practitioners inferring causality from observational data usually rely on a single method and treat its output as causal truth. Recent tools select an optimal method for a dataset, and recent ensembles aggregate multiple causal-discovery algorithms into one graph, but little work pools evidence across different mathematical traditions, including non-causal ones. We present Multi-Method Causal Evidence Synthesis (MCES), a framework that ranks which candidate drivers in an observational system are most likely relevant to a set of outcomes, and with what strength of evidence. MCES runs eleven methods across eight mathematical traditions on observational panel data and pools their outputs into a Convergent Evidence Score (CES), a linear opinion pool. CES quantifies convergence of evidence across analytical lenses: the degree to which methods with different assumptions point to the same driver-outcome relationship. It does not claim causal identification in the interventionist sense; it supports hypothesis prioritization, not a transferable probability of causation. MCES first applies Structural-Behavioral Decomposition to remove definitional (algebraic) relationships, then runs all methods, normalizes outputs to [0,1], and pools them. We distinguish MCES from method selection, structural ensembles, prediction ensembles, and literature synthesis. Using synthetic data with embedded ground truth, the Sachs protein-signaling benchmark, six Bayesian-network structure benchmarks, and two further synthetic domains, we show MCES ranks true edges near the top (Precision@5 = 1.0, Precision@10 = 0.96 on the primary scenario), with a low empirical rate of null pairs reaching Moderate-or-higher convergence. Our central point is not that the pool beats every individual method, but that no single method is uniformly best across the evaluated scenarios, so MCES offers a method-agnostic default.
Bayesian network structure learning (BNSL) from observational data struggles with orientation identifiability, while large language models (LLMs) offer broad but often unreliable causal knowledge. We propose combining these complementary sources through a novel representation, termed Probabilistic Dependency Graphs (PDGs). In a PDG, each edge is associated with a distribution over directed, undirected, and absent states, enabling fusion via weighted averaging. We evaluate this approach on 26 benchmark networks, combining ensembles of three BNSL algorithms (FGES, Tabu, PC) with three LLMs (Gemini, Claude, GPT) across multiple prompts and random seeds. A simple 50/50 fusion improves F1 over the better of either source alone in 22 of 26 networks, with a statistically significant mean improvement of $0.056$ $(p<0.001)$. Analysis reveals that the two sources play complementary roles: BNSL contributes a high-recall edge skeleton (80\% vs 60\% for LLM), while LLM contributes accurate edge orientation (96\% vs 77\% for BNSL). Our results show that representing both sources as probabilistic uncertainty over edge existence and orientation is a practical and effective way to improve causal graph accuracy.
Jonas Braun, Fabian Fischbach, Daniel Köglmayr +2cs.LG
Machine learning methods predict many real-world systems with remarkable accuracy, but they are typically treated as black boxes that offer no insight into which interactions drive the dynamics. Causal discovery methods reconstruct the interaction network from observational data, but without regard to whether the inferred structure supports prediction. Existing approaches combining both tasks rely on a single global hyperparameter, such as a causal threshold or a fixed neighborhood size, which cannot recover the structure of heterogeneous systems. Here we introduce causal local states (CLS), a framework that simultaneously infers an approximate Granger-causal interaction network and forecasts the system dynamics. For each node independently, we select the smallest set of neighbors that allows a predictive model to forecast the node near-optimally, and the resulting neighborhoods are then combined for a forecast of the full system. On three benchmarks of increasing difficulty, we achieve reconstruction of the underlying networks with high fidelity and forecasts on par with a model that is supplied with the true network, providing a step toward explainable and scalable forecasting of complex systems.
Recovering the directed acyclic graph (DAG) of a structural equation model (SEM) from observational data is a central problem in causal discovery. The iterative gradient descent and per-problem hyperparameter tuning of continuous-optimization methods are poorly suited to two practically important regimes: the sample-limited regime, where the number of samples is comparable to or smaller than the number of nodes in the DAG, and the compute-limited regime. This work proposes SURE-Ridge, a non-iterative, closed-form estimator for equal variance linear Gaussian SEM. The method performs parallel node-wise regressions with regularization parameters chosen adaptively by Stein's unbiased risk estimate (SURE), and applies an adaptive thresholding procedure to extract a DAG from the resulting soft adjacency matrix. Numerical results show that SURE-Ridge achieves the lowest structural Hamming distance in the small-sample regime and the lowest run time across all sample sizes tested, compared with NOTEARS, DAGMA, and GBNSL baselines.
Pavel Averin, Theodoros Moysiadis, Ioannis Katakisstat.ME stat.ML
Constraint-based causal discovery like PC and FCI depends on its conditional independence test. Partial correlation and the Generalised Covariance Measure (GCM) detect only the conditional covariance of residuals, so they miss dependence in the mean's nonlinear part, the scale, and the tails. Tests that detect more are biased inside PC, not scalable, only continuous, or not aimed at the tails. Our Generalised Feature Covariance Measure (GFCM) is valid, sensitive beyond covariance, robust inside PC, and applicable to mixed-type data. It runs the GCM template on a configurable set of residual features with conditional mean zero (centered moments and conditional quantile indicators), pooled in blocks and combined by the Cauchy rule, with a growing-knot spline nuisance at regression cost. We contribute (i) a centering result making the scale feature Neyman orthogonal, where the uncentered version is biased; (ii) the orientation asymmetry the mean-quantile construction creates inside PC, and its fix; (iii) a Phi-faithfulness theory under which PC with GFCM recovers the CPDAG of the set's detection class; and (iv) a benchmark of CI tests sensitive beyond covariance on synthetic data, semi-synthetic tail injections, and PC discovery on random DAGs. Under size-corrected power, GFCM recovers the scale and tail edges the covariance family misses and alone keeps power at the deep conditioning sets PC issues. It stays calibrated as n grows, whereas FFCI, the boosted GCM, and the partial copula test do not, and it handles mixed-type data directly. Inside PC at scale it attains the lowest skeleton SHD among tests that stay calibrated, while the others inflate false edges. Validity rests on an additive nuisance, and the tail advantage is shown on simulated and semi-synthetic data, as no fully real benchmark with both heavy tails and known structure exists.
Cixuan Zhang, Guy Van den Broeck, Benjie Wangcs.LG cs.AI stat.ML
Causal discovery aims to uncover the underlying causal relationships given data generated from a system. The goal, however, is not merely to predict causal edges given data, but also to be able to interpret and explain either observed or hypothesized phenomena, such as a particularly large causal effect. We consider this task of conditional causal discovery and cast it as a Bayesian inference problem, in which we target the posterior over causal graphs and parameters conditional on an event such as a causal-effect constraint. Unfortunately, this poses a computational challenge: existing approaches to Bayesian causal discovery struggle when the event has small posterior mass. To address this, we adapt rare-event estimation techniques to perform inference the joint graph-parameter space. Our method gradually drives a particle population toward the constrained region while maintaining samples that approximate the conditional posterior. Empirical evaluation on synthetic graphs validates the accuracy of our approach at small and large scales, and we show in a case study on the Sachs protein dataset how our method can be used to aid scientific exploration by providing pathway-level summaries.
Pavel Averin, Theodoros Moysiadis, Ioannis Katakisstat.ML cs.LG
Conditional Independence (CI) tests are the statistical engine of constraint-based causal discovery: in algorithms such as PC (Peter-Clark) and FCI (Fast Causal Inference), skeleton pruning and key orientations follow directly from CI decisions. This survey reviews CI testing with emphasis on assumptions, robustness, and scalability in high-dimensional and mixed-type settings common in biomedical domains. The survey organizes widely used CI methods into six families: partial-correlation, contingency-table, regression, nearest-neighbor, kernel, and machine-learning-based. Special emphasis is provided on the robustness layers that address the limitations of these families. For each family, the survey examines when CI decisions reflect the data-generating distribution and when they fail. By this, we link test-level properties, including power decay with conditioning set size and asymmetric type I/II error consequences, to graph-level errors in skeleton recovery and v-structure orientation. The survey also compares adoption across major R and Python libraries and summarizes open challenges, including mixed-type CI testing without discretization, small-sample error control, and strategies for improving scalability of CI-testing.
Bayesian causal discovery seeks to determine the posterior distribution of causal theories, which are interpreted as directed acyclic graphs (DAGs) that explain the observed data. The resulting posterior allows systematic reasoning regarding epistemic uncertainty within these theories. Nonetheless, finding such graphs is difficult due to identifiability problems and limited observational data. Furthermore, precisely approximating posterior over graphs is challenging given vast range of potential DAGs. Recent Bayesian approaches have addressed some of these challenges, yet they remain limited as they fail to encode dependencies between edges, and lack principled ways to incorporate domain knowledge as inductive biases during the search process. To overcome these limitations, we propose SVI-DAG, a structured variational inference approach to Bayesian causal discovery using observational data and prior beliefs that uses normalizing flows to model dependencies between edges, supporting expressive and multimodal posterior learning over DAGs. To mitigate mode seeking behaviour in evidence lower bound optimization and promote mode coverage, we use stein variational gradient descent to update the node potentials using a kernel in acyclicity space. We evaluate SVI-DAG against 5 state-of-the-art Bayesian DAG learning methods and demonstrate superior performance in uncertainty quantification while remaining competitive in terms of structural accuracy.
Abhinav Thorat, Ravi Kumar Kolla, Vishak K Bhat +2cs.LG cs.AI
Causal Discovery (CD) from observational data faces two fundamental challenges. First, purely statistical methods often lack the power to resolve structural ambiguities in low-sample regimes. Second, although LLM-assisted hybrid approaches improve structure recovery through semantic reasoning, the influence of that reasoning on individual edge decisions remains largely opaque. Consequently, existing hybrid methods fail to satisfy a fundamental requirement: explaining why a particular edge is included or excluded in the learned directed acyclic graph (DAG). This is critical in real-world applications, where no ground-truth DAG exists and every structural decision must be independently justified. We formalize this requirement as decision traceability, requiring every inferred edge to be supported by auditable statistical evidence, Markov Blanket consistency, or explicit domain reasoning. We propose GENESIS, an explainable hybrid CD framework that decomposes graph construction into interpretable decision points. GENESIS first identifies and scores three-node structural motifs, including chains, forks, and colliders, to establish transparent structural priors, then progressively refines the graph by integrating these priors with observational evidence, invoking domain knowledge only when statistical evidence is insufficient. By design, every edge decision is resolved through an auditable source of evidence. Experiments show that GENESIS achieves 100% decision traceability across all settings, establishing explainability as a first-class objective in causal discovery. Despite this additional requirement, GENESIS consistently outperforms purely statistical CD methods on the majority of benchmark datasets across all sample regimes in terms of Structural Hamming Distance (SHD), while achieving performance comparable to state-of-the-art LLM-assisted approaches.
Nitish Nagesh, Elahe Khatibi, Thomas Dean Hughes +3cs.LG
Causal discovery recovers directed structure from observational data and is increasingly used in clinical settings to support mechanism reasoning and fairness audits of predictive models. Path-specific counterfactual fairness asks whether a protected attribute influences an outcome through illegitimate pathways, but these estimands are defined relative to a supplied causal graph and therefore inherit whatever errors the discovery step introduces. Discovery methods are routinely scored on aggregate structural metrics that weight all edges equally, and no established evaluation asks whether the specific pathway an audit depends on survives discovery---or what the audit reports when that pathway is missing. Here we show that full-graph Graph-of-Thoughts reasoning yields acyclic discovered graphs that are structurally competitive with large language model (LLM) baselines, yet that structural fidelity alone does not guarantee fairness-faithful audits. We introduce GoT-CD, in which the reasoning unit is a complete candidate edge set: multiple graphs are generated in parallel, scored by a deterministic validity function, and merged under a hard union constraint that forbids invented edges, with greedy projection enforcing a DAG before commitment. GoT-CD returns a valid DAG on all five reported benchmarks and achieves the best DAG-valid F1 score among LLM methods on Asia, Alzheimer's, and COVID-Respiratory datasets. On an Alzheimer's benchmark with known unfair path, a post-hoc path-specific audit shows that five of eight discovered graphs recover no path from the sensitive attribute to the outcome and therefore report a null overall effect while mediated effects persist, necessitating downstream path-specific fairness analysis along with structural discovery.
Marco Ruiz, Miguel Arana-Catania, David R. Ardila +1cs.LG
Environmental time-series causal discovery requires expert decisions about method choice, conditional-independence tests, lag horizons, sample-size adequacy, multiple-testing control, and evidence interpretation. Applied inconsistently across datasets, these choices yield graphs that cannot be compared, reproduced, or audited. We present AutoCause, an open-source Python workflow that records each decision, derives defaults from an extended causal-audit module, and admits domain-informed overrides. The workflow wraps four established causal-discovery methods from three families, adds non-causal reference models, and grades links by method-count support. On 145 datasets from DGP-Atlas, TimeGraph, and a topology-derived CausalRivers reference, the methods recover complementary parts of the reference graphs. Majority-supported links are more precise than single-method links on the synthetic benchmarks but not against river topology. AutoCause converts inconsistent expert practice into an auditable, repeatable analysis; causal interpretation remains with the analyst. Available at https://github.com/marcoruizrueda/autocause.
Causal discovery in multivariate time series data is challenging due to complex interactions, high dimensionality, and nonlinear dependencies among variables. Existing methods often struggle to capture these complexities, resulting in inaccurate causal structures. To address this issue, we propose a novel framework that leverages self-attention mechanisms within the transformer architecture for causal discovery. Our approach introduces a novel inverted causal self-attention mechanism (CSAM) that emphasizes latent and indirect causal relationships by inverting tokens and inducing sparsity in attention scores, focusing on significant causal interactions and reducing spurious correlations. Additionally, we develop a global causal algorithm to identify global causal links, providing a holistic metric for causal influence, along with a causal verification module to ensure robustness in the identified causal relationships, enhancing the reliability of our framework. Experiments on both linear and nonlinear datasets, along with ablation studies and sensitivity analyses, show that our framework outperforms existing methods, demonstrating its potential for causal discovery in complex multivariate time series.
Modern telecommunication, cloud, and microservice systems emit correlated alarm cascades when components fail. Root cause analysis (RCA) aims to identify the small set of alarms that initiate each cascade. A common approach learns a causal graph from observational logs and predicts all zero-in-degree alarms in each incident-induced subgraph. However, the learned graph remains fixed and cannot benefit from expert diagnoses of historical incidents. We close this loop with EvoCause. Expert labels constrain which alarms should be source nodes but do not specify the edge edits needed to satisfy those constraints. EvoCause uses a large language model (LLM) to propose semantically plausible graph edits, while deterministic code validates node identities and acyclicity and retains the best graph on a labeled alignment set. At test time, the refined graph alone produces transparent predictions without an LLM call. We also release TeleRCA, an expert-annotated benchmark from a production telecommunication network containing $485{,}681$ alarm events spanning $194$ alarm types over $5{,}621$ resources. On synthetic data, EvoCause initialized with the PC causal discovery algorithm outperforms the unrefined PC baseline, raising Node F1, Case EM, and Graph F1 by $11.59$, $9.40$, and $4.59$ percentage points, respectively, while reducing nSHD by $0.2379$. On TeleRCA, replacing human-readable alarm titles with anonymous identifiers lowers Node F1 and Case EM by $6.12$ and $8.04$ percentage points, respectively, indicating that alarm-name information contributes to graph refinement.
The problem of learning the graphical Markov blanket (MB) of a variable from data has applications in many areas such as structure learning for Bayesian networks and Markov random fields, causal discovery, and feature selection. However, a common assumption most methods make is that the conditional independencies in the distribution imply the same separation in the graphical structure -- also known as the faithfulness assumption. Unfortunately, this assumption can be violated by higher-order dependencies such as XOR and parity-type relations, and -- on finite samples -- by empirical violations that, in extreme cases, even induce spurious dependencies absent from the true distribution. Therefore, in this paper we propose a "k-order" relaxation of the faithfulness assumption that captures parity type relationships between k+2 variables. We then propose a proof of concept algorithm called k-order Markov blanket (kOMB) that uses this relaxation for MB discovery. Finally, we empirically show how kOMB can recover the MB of a variable under both true and empirical violations of faithfulness. Code available at: https://github.com/lklee9/k-order-Markov-blanket
We describe Causal-TS, an open-source Python library for causal discovery in high-dimensional and nonstationary multivariate time series. Causal-TS provides four specialized algorithms-CDNOTS, CDNOTS+, CEDAR, and GRACE-along with wrappers for GES, Granger, LASSO-VAR, and LGES, all sharing a unified conditional independence (CI) test layer with GPU acceleration via PyTorch. A regime discovery pipeline detects structural breaks via pluggable changepoint detectors and runs discovery per regime with regime-specific parameters. A command-line interface, synthetic data generators, and optional DoWhy integration provide an end-to-end pipeline from raw time series to causal effect estimates. The library is pip-installable, tested on Python 3.10--3.12, and available at https://github.com/bloomberg/causal-ts.
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.
We propose CEDAR (Causal Edge Discovery for Autoregressive Processes), a constraint-based method for lagged causal edge discovery in sparse autoregressive time series. CEDAR screens candidate cross-variable lags using AR(1)-residualized, U-centered distance correlation, then applies two targeted conditional-independence tests per significant cross-variable lag candidate and accepts at most one lag per ordered pair. A stable MCI pruning step removes indirect edges, and optional deterministic C-nodes adjust for specified trend-like nonstationarity. In sparse regimes where few lags survive screening, CEDAR requires $O(d^2)$ CI tests after screening while retaining edge-level interpretability. CEDAR is most effective when data are scarce and variables exhibit lag-1 self-dynamics; methods with richer conditioning sets become preferable as $T$ grows or when higher-order autoregressive or simultaneous multi-lag effects are common.
Discovering the direct causes and effects of a target variable from observational data is a fundamental problem in causal discovery, with broad applications in domains such as gene regulatory analysis and biomedical research. Existing causal discovery methods either learn a global causal structure, which incurs substantial computational cost, or assume the absence of latent variables and selection bias, assumptions that are often violated in real-world settings. Motivated by these challenges, we study local causal structure learning in the presence of latent variables and selection bias. Specifically, we first characterize a local region that enables target-specific causal discovery without recovering the entire global structure. We then establish a theoretical bridge between causal information learned from the observed distribution induced on this local region and the corresponding information in the global causal structure. Building on these foundations, we propose LoCaLS, a local causal structure learning algorithm that is sound and complete under standard assumptions and identifies the same direct causes and effects of a target variable as those identifiable by global causal discovery methods, while allowing for latent variables and selection bias. Extensive experiments on random and real-world structures demonstrate that the proposed method consistently achieves higher structural accuracy than existing local methods while requiring substantially less computational effort than state-of-the-art global methods. Furthermore, applications to two real-world gene expression datasets reveal biologically plausible target-specific causal structures, demonstrating its practical applicability in large-scale biological data analysis.
Causal discovery methods have shown strong performance in temporal systems, but they typically rely on regular and discrete lag structures, limiting their applicability to regularly sampled data. However, many real-world tasks require dealing with irregularly sampled streams of events, such as sensor streams, healthcare data, and financial transactions. In this work, we propose an extension of PCMCI+, a state-of-the-art method for causal discovery on regular multivariate time series, to allow for handling irregular time series. Instead of modelling causal relations through fixed-lag dependencies, our method aggregates causal influence over predefined temporal windows. We evaluate our method on synthetic irregular event streams with known causal structures under different signal-to-noise ratios, showing that it consistently recovers the underlying causal graph and substantially outperforms the standard PCMCI+ on irregularly sampled data.
Causal discovery from observational tabular data remains fundamentally challenging, primarily due to the heterogeneity of underlying causal mechanisms and the high-dimensional combinatorial search space of Directed Acyclic Graphs (DAGs). In this paper, we propose \textbf{DAG-FM}, a novel foundation model architecture that amortizes causal discovery. Unlike direct matrix prediction, DAG-FM decomposes the causal discovery process into two auto-regressive stages using two specialized Transformer-based sub-modules: a leaf-node predictor and a parent-node predictor. To effectively model complex row-column interactions, we adopt a robust tabular interaction block to output feature-wise representations. Crucially, to handle diverse and unknown Functional Causal Model (FCM) assumptions in real-world scenarios, we introduce Mixture-of-Leaf-Experts (MoLE), allowing the model to dynamically route and adapt to identifiable mechanism families. Through an iterative inference algorithm, DAG-FM seamlessly extracts causal orderings and constructs valid DAGs. Extensive experiments demonstrate that DAG-FM achieves state-of-the-art performance on both synthetic benchmarks and complex real-world datasets, significantly outperforming traditional classical algorithms and recent foundation models in both accuracy and scalability.