Learning Cross-Domain Representations for Transferable Drug Perturbations on Single-Cell Transcriptional Responses
Hui Liu, Shikai Jin
摘要
Phenotypic drug discovery has attracted widespread attention because of its potential to identify bioactive molecules. Transcriptomic profiling provides a comprehensive reflection of phenotypic changes in cellular responses to external perturbations. In this paper, we propose XTransferCDR, a novel generative framework designed for feature decoupling and transferable representation learning across domains. Given a pair of perturbed expression profiles, our approach decouples the perturbation representations from basal states through domain separation encoders and then cross-transfers them in the latent space. The transferred representations are then used to reconstruct the corresponding perturbed expression profiles via a shared decoder. This cross-transfer constraint effectively promotes the learning of transferable drug perturbation representations. We conducted extensive evaluations of our model on multiple datasets, including single-cell transcriptional responses to drugs and single-and combinatorial genetic perturbations. The experimental results show that XTransfer-CDR achieved better performance than current state-of-theart methods, showcasing its potential to advance phenotypic drug discovery.
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- Predicting Cellular Responses to Novel Drug Perturbations at a Single-Cell ResolutionLeon Hetzel, Simon Böhm, Niki Kilbertus, Stephan Günnemann 等NeurIPS 2022 · 被引用 125 次
- DRANet: Disentangling Representation and Adaptation Networks for Unsupervised Cross-Domain AdaptationSeunghun Lee, Sunghyun Cho, Sunghoon ImCVPR 2021
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