arXiv:2410.13956cs.LG
Benchmarking Transcriptomics Foundation Models for Perturbation Analysis : one PCA still rules them all
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Abstract
Understanding the relationships among genes, compounds, and their interactions in living organisms remains limited due to technological constraints and the complexity of biological data. Deep learning has shown promise in exploring these relationships using various data types. However, transcriptomics, which provides detailed insights into cellular states, is still underused due to its high noise levels and limited data availability. Recent advancements in transcriptomics sequencing provide new opportunities to uncover valuable insights, especially with the rise of many new foundation models for transcriptomics, yet no benchmark has been made to robustly evaluate the effectiveness of these rising models for perturbation analysis. This article presents a novel biologically motivated evaluation framework and a hierarchy of perturbation analysis tasks for comparing the performance of pretrained foundation models to each other and to more classical techniques of learning from transcriptomics data. We compile diverse public datasets from different sequencing techniques and cell lines to assess models performance. Our approach identifies scVI and PCA to be far better suited models for understanding biological perturbations in comparison to existing foundation models, especially in their application in real-world scenarios.
Yes, this. A lot of work in this field is missing from that timeline. Just circa 2010-2020, Les Loew's VCell 3D PDE approaches, Faeder et al.'s BioNetGen / ODE work, Luthey-Schulten Shulten's grid based cell models, the Pittsburgh supercomputing center's 3D monte-carlo MCell…
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