RAPTORGraph: graph-based pathway modeling for causal discovery in single-cell perturbations
- 1Institute of Information Processing, Leibniz University Hannover, Hannover, Germany
Abstract
Experiments involving the perturbation of individual cells are central to understanding cellular mechanisms and can accelerate drug discovery. Causal representation learning allows us to uncover the latent factors that regulate biological systems and predict the impact of novel perturbations. Unfortunately, existing methods fail to address intervention spillover in a closed-world setting where intervention targets are known a priori, such as in Perturb-seq experiments, due to their reliance on dense encoders. Furthermore, incorporating curated biological pathways into the model imposes a confirmatory bias, forcing it to explain the data through preexisting pathways and reducing the set of hypotheses the model can explore, while discarding novel signals that lie outside the annotated pathways. In this work, we introduce RAPTORGraph, a {beta}-variational autoencoder with a GraphPathway encoder that explicitly models complex gene-to-gene interactions within learned pathways. Moreover, our model's preconditioning isolates the influence of perturbed genes, yielding clean, single-node latent interventions required for identifiable causal discovery and eliminating spillover. Finally, we train the model on data preprocessed with optimal-transport alignment, which guarantees a well-defined mapping between control and perturbed samples and further stabilizes the learned latent representations. We demonstrate that RAPTORGraph improves state-of-the-art performance on downstream analyses of unseen perturbations, such as non-additive interactions, while performing competitively on objective metrics, such as mean squared error and maximum mean discrepancy. The source code is available at https://github.com/sXperfect/RAPTORGraph.
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BibTeX
@misc{adhisantoso2026raptorgraph,
title = {{RAPTORGraph: graph-based pathway modeling for causal discovery in single-cell perturbations}},
author = {Y. G. Adhisantoso and S. K. Schröder and M. Gress and M. Hernaez and J. Voges},
howpublished = {bioRxiv},
year = {2026},
month = nov,
doi = {10.64898/2026.11.03.763980},
url = {https://www.biorxiv.org/content/10.64898/2026.11.03.763980v1},
note = {CC BY},
}
RIS
TY - UNPB
TI - RAPTORGraph: graph-based pathway modeling for causal discovery in single-cell perturbations
AU - Y. G. Adhisantoso
AU - S. K. Schröder
AU - M. Gress
AU - M. Hernaez
AU - J. Voges
PY - 2026
DA - 2026/11/03
PB - bioRxiv
DO - 10.64898/2026.11.03.763980
UR - https://www.biorxiv.org/content/10.64898/2026.11.03.763980v1
AB - Experiments involving the perturbation of individual cells are central to understanding cellular mechanisms and can accelerate drug discovery. Causal representation learning allows us to uncover the latent factors that regulate biological systems and predict the impact of novel perturbations. Unfortunately, existing methods fail to address intervention spillover in a closed-world setting where intervention targets are known a priori, such as in Perturb-seq experiments, due to their reliance on dense encoders. Furthermore, incorporating curated biological pathways into the model imposes a confirmatory bias, forcing it to explain the data through preexisting pathways and reducing the set of hypotheses the model can explore, while discarding novel signals that lie outside the annotated pathways. In this work, we introduce RAPTORGraph, a {beta}-variational autoencoder with a GraphPathway encoder that explicitly models complex gene-to-gene interactions within learned pathways. Moreover, our model's preconditioning isolates the influence of perturbed genes, yielding clean, single-node latent interventions required for identifiable causal discovery and eliminating spillover. Finally, we train the model on data preprocessed with optimal-transport alignment, which guarantees a well-defined mapping between control and perturbed samples and further stabilizes the learned latent representations. We demonstrate that RAPTORGraph improves state-of-the-art performance on downstream analyses of unseen perturbations, such as non-additive interactions, while performing competitively on objective metrics, such as mean squared error and maximum mean discrepancy. The source code is available at https://github.com/sXperfect/RAPTORGraph.
ER -