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Season combinatorial intervention predictions with Salt & Peper
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Interventions play a pivotal role in the study of complex biological systems. In drug discovery, genetic interventions (such as CRISPR base editing) have become central to both identifying potential therapeutic targets and understanding a drug's mechanism of action. With the advancement of CRISPR and the proliferation of genome-scale analyses such as transcriptomics, a new challenge is to navigate the vast combinatorial space of concurrent genetic interventions. Addressing this, our work concentrates on estimating the effects of pairwise genetic combinations on the cellular transcriptome. We introduce two novel contributions: Salt, a biologically-inspired baseline that posits the mostly additive nature of combination effects, and Peper, a deep learning model that extends Salt's additive assumption to achieve unprecedented accuracy. Our comprehensive comparison against existing state-of-the-art methods, grounded in diverse metrics, and our out-of-distribution analysis highlight the limitations of current models in realistic settings. This analysis underscores the necessity for improved modelling techniques and data acquisition strategies, paving the way for more effective exploration of genetic intervention effects.
Forward citations
Cited by 3 Pith papers
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Interpretable Causal Representation Learning for Biological Data in the Pathway Space
SENA-discrepancy-VAE combines a pathway-masked encoder with discrepancy-VAE, giving causal latent factors interpretable as biological process combinations with comparable unseen-perturbation prediction.
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No Foundations without Foundations -- Why semi-mechanistic models are essential for regulatory biology
A semi-mechanistic model of CRISPR perturbation screens, built from editing, media, and waiting operations, improves gene-expression prediction when trained with an extra steady-state constraint.
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Active learning for efficient discovery of optimal gene combinations in the combinatorial perturbation space
NAIAD uses single-gene effects plus adaptive embeddings and maximum-predicted-effect sampling to discover the strongest gene pairs in combinatorial CRISPR screens with fewer experimental rounds.
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