Researcher profile

Anish Dhir

Anish Dhir contributes to research discovery and scholarly infrastructure.

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Published work

2 published item(s)

preprint2026arXiv

PRIM: Meta-Learned Bayesian Root Cause Analysis

Root cause analysis (RCA) in complex systems is challenging due to error propagation across multiple variables, the need for structural causal knowledge, and the computational cost of inference at test time. We introduce PRIM (Prior-fitted Root cause Identification with Meta-learning), a causal meta-learning approach that frames RCA as a Bayesian inference task over a synthetic prior of causal models. By marginalising out structural uncertainty, PRIM implicitly identifies changes in the data-generating mechanism between baseline and anomalous periods. In doing so, PRIM infers distributional differences without explicit statistical testing, and implicitly learns causal structure without model fitting at test time. Following the simulation-based meta-learning paradigm of prior-fitted networks, PRIM uses a Model-Averaged Causal Estimation (MACE) transformer neural process that jointly attends over observational and anomalous samples and the causal structure of nodes, enabling zero-shot inference in 17,ms for systems with up to 100 variables. Across synthetic benchmarks and two realistic benchmark datasets, PetShop and CausRCA, PRIM is competitive with methods that are aware of the system's causal graphical structure a priori while outperforming graph-unaware methods on several tasks. Lightweight fine-tuning to specific domains and data dynamics improves performance further.

preprint2022arXiv

Generalization bounds and algorithms for estimating conditional average treatment effect of dosage

We investigate the task of estimating the conditional average causal effect of treatment-dosage pairs from a combination of observational data and assumptions on the causal relationships in the underlying system. This has been a longstanding challenge for fields of study such as epidemiology or economics that require a treatment-dosage pair to make decisions but may not be able to run randomized trials to precisely quantify their effect and heterogeneity across individuals. In this paper, we extend (Shalit et al, 2017) to give new bounds on the counterfactual generalization error in the context of a continuous dosage parameter which relies on a different approach to defining counterfactuals and assignment bias adjustment. This result then guides the definition of new learning objectives that can be used to train representation learning algorithms for which we show empirically new state-of-the-art performance results across several benchmark datasets for this problem, including in comparison to doubly-robust estimation methods.