DINOcell: Learning Generalizable Perturbation Effects through Self-Distillation
Jonathan LiiD, Nilgun TasdemiriD, Sofia Kyriazopoulou-Panagiotopoulou, Sophie Xu, Allyson J. MerrelliD, Josephine Susanto, Ashley A. Cass, David DeTomaso, Holly Steach, Julie C. ChowiD, Li Wang, Neal G. RavindraiD, Aram Kang, Grace X. Y. ZhengiD, Mary Chua, Per Knudsgaard, Emmie He, Fabio Ingrao, Angela C. BoroughsiD, Brie Copperman, Nia Charrington, Kathryn Abboud, Lionel BerthoiniD, Daniel Baca, Lina M LeóniD, , Amaro N Taylor-WeineriD
Abstract
AO_SCPLOWBSTRACTC_SCPLOWPredicting cellular responses to therapeutics is a promising approach for novel target discovery. However, state-of-the-art computational models designed to predict perturbation effects struggle to generalize and outperform simple baselines. We present DINOcell, a weakly supervised framework that adapts self-distillation to single-cell transcriptomics for predicting perturbation effects. We demonstrate that DINOcell outperforms baselines in predicting the effects of single gene perturbations. Furthermore, DINOcell accurately predicts non-additive effects of combination perturbations, indicating its capacity to model complex genetic interactions. Finally, we show that DINOcell learns representations that capture biological signals and is a promising, generalizable approach for in silico perturbation modeling, providing a valuable tool for accelerating therapeutic target discovery.
02 /Specification & Classification
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