Predicting perturbation targets with causal differential networks

• URL: http://arxiv.org/abs/2410.03380v1
• Date: Fri, 4 Oct 2024 12:48:21 GMT
• Title: Predicting perturbation targets with causal differential networks
• Authors: Menghua Wu, Umesh Padia, Sean H. Murphy, Regina Barzilay, Tommi Jaakkola,
• Abstract summary: We use an amortized causal discovery model to infer causal graphs from the observational and interventional datasets. We learn to map these paired graphs to the sets of variables that were intervened upon, in a supervised learning framework. This approach consistently outperforms baselines for perturbation modeling on seven single-cell transcriptomics datasets.
• Score: 23.568795598997376
• License: http://creativecommons.org/licenses/by/4.0/
• Abstract: Rationally identifying variables responsible for changes to a biological system can enable myriad applications in disease understanding and cell engineering. From a causality perspective, we are given two datasets generated by the same causal model, one observational (control) and one interventional (perturbed). The goal is to isolate the subset of measured variables (e.g. genes) that were the targets of the intervention, i.e. those whose conditional independencies have changed. Knowing the causal graph would limit the search space, allowing us to efficiently pinpoint these variables. However, current algorithms that infer causal graphs in the presence of unknown intervention targets scale poorly to the hundreds or thousands of variables in biological data, as they must jointly search the combinatorial spaces of graphs and consistent intervention targets. In this work, we propose a causality-inspired approach for predicting perturbation targets that decouples the two search steps. First, we use an amortized causal discovery model to separately infer causal graphs from the observational and interventional datasets. Then, we learn to map these paired graphs to the sets of variables that were intervened upon, in a supervised learning framework. This approach consistently outperforms baselines for perturbation modeling on seven single-cell transcriptomics datasets, each with thousands of measured variables. We also demonstrate significant improvements over six causal discovery algorithms in predicting intervention targets across a variety of tractable, synthetic datasets.

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