Causal Effect Inference for Structured Treatments
About
We address the estimation of conditional average treatment effects (CATEs) for structured treatments (e.g., graphs, images, texts). Given a weak condition on the effect, we propose the generalized Robinson decomposition, which (i) isolates the causal estimand (reducing regularization bias), (ii) allows one to plug in arbitrary models for learning, and (iii) possesses a quasi-oracle convergence guarantee under mild assumptions. In experiments with small-world and molecular graphs we demonstrate that our approach outperforms prior work in CATE estimation.
Jean Kaddour, Yuchen Zhu, Qi Liu, Matt J. Kusner, Ricardo Silva• 2021
Related benchmarks
| Task | Dataset | Result | Rank | |
|---|---|---|---|---|
| pancytopenia onset prediction | Claims | Rate0.00e+0 | 60 | |
| Causal effect prediction | Medical claims pancytopenia occurrence (test) | Rate @ 0.9990.00e+0 | 15 | |
| CATE estimation | Claims dataset (test) | Rate @ 0.9990.00e+0 | 15 | |
| Causal effect prediction | LINCS 20 DEGs (unseen perturbation/cell-line) | PEHE4.06 | 8 | |
| Causal effect prediction | LINCS 50 DEGs (unseen perturbation cell-line) | PEHE3.78 | 8 | |
| CATE estimation | SW (In-sample) | WPEHE@623 | 5 | |
| CATE estimation | SW (Out-sample) | WPEHE@623.19 | 5 | |
| CATE estimation | TCGA (In-sample) | WPEHE@610.98 | 5 | |
| CATE estimation | TCGA (Out-sample) | WPEHE@68.15 | 5 |
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