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Benchmarking Transcriptomics Foundation Models for Perturbation Analysis : one PCA still rules them all

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arxiv 2410.13956 v2 pith:I6T5W7ID submitted 2024-10-17 cs.LG stat.ML

classification cs.LGstat.ML
keywords modelstranscriptomicsdatafoundationanalysisperturbationbiologicalespecially
verification ladder T0 review T1 audit T2 compute T3 formal
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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.

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Cited by 3 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Diversity by Design: Addressing Mode Collapse Improves scRNA-seq Perturbation Modeling on Well-Calibrated Metrics

    q-bio.GN 2025-06 conditional novelty 6.0 of 10

    A systematic control bias inflates mean-baseline performance in scRNA-seq perturbation benchmarks, and the proposed DEG-weighted metrics with an all-perturbed-cells reference yield null mean-baseline performance while...

  2. TxPert: Leveraging Biochemical Relationships for Out-of-Distribution Transcriptomic Perturbation Prediction

    cs.LG 2025-05 conditional novelty 6.0 of 10

    TxPert uses graph neural networks over multiple gene interaction graphs to predict transcriptional responses to unseen single, double, and cross-cell-line perturbations, outperforming GEARS and scLAMBDA in benchmark tests.

  3. Virtual Cells: Predict, Explain, Discover

    cs.LG 2025-05 conditional novelty 6.0 of 10

    A perspective proposing that therapeutically useful virtual cells must predict, explain, and discover, with a framework of capabilities and performance levels to guide their development.

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