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This research introduces DI-MIL, a training-free module that decomposes standard image tiles into multiple weighted instances to preserve fine-grained diagnostic signals in weakly supervised whole slide image classification. By decoupling encoding context from instance granularity, the method significantly outperforms existing Multiple Instance Learning baselines without requiring architectural changes or re-encoding overhead. The approach effectively addresses the dilution of sparse diagnostic evidence common in cytopathology tasks using frozen foundation models.
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One Tile, Multiple Instances: Rethinking MIL for Sparse Diagnostic Evidence

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arXiv:2610.04853v1 Announce Type: cross Abstract: In weakly supervised Whole Slide Image (WSI) classification, feature extractors typically compress each image tile into a single global embedding. Consequently, slide-level aggregators are restricted to this coarse tile scale, concealing fine-grained sub-tile evidence from the attention mechanism. We introduce DI-MIL, a framework that decouples encoding context from instance granularity through decomposed instances. By clustering dense spatial tokens from a frozen foundation model within each tile, DI-MIL converts a single tile into multiple independently weighted instance embeddings. As a training-free post-encoding module, DI-MIL integrates seamlessly into existing pipelines without requiring re-encoding or downstream architectural modifications. We evaluate DI-MIL on cytopathology, a challenging testbed where sparse diagnostic signals are easily diluted within standard tiles. Across four datasets, three frozen foundation models, and two attention-based aggregators, DI-MIL demonstrates consistent efficacy, improving 67 of 72 metric-level comparisons, with the largest mean gains reaching 3.64 points under cytopathology-specific backbones. In a broader comparison against seven representative MIL baselines, DI-MIL paired with ACMIL achieves highest mean performance in 33 of 36 backbone-dataset-metric comparisons. Ablations show that direct smaller tiling inflates the extracted tile count by up to 43.3$\times$ with non-monotonic performance, whereas DI-MIL incurs zero additional image-extraction overhead while achieving the strongest overall results. These results establish instance construction as an orthogonal design dimension in MIL, supporting DI-MIL as a cost-efficient solution under sparse diagnostic evidence.

Abstract:In weakly supervised Whole Slide Image (WSI) classification, feature extractors typically compress each image tile into a single global embedding. Consequently, slide-level aggregators are restricted to this coarse tile scale, concealing fine-grained sub-tile evidence from the attention mechanism. We introduce DI-MIL, a framework that decouples encoding context from instance granularity through decomposed instances. By clustering dense spatial tokens from a frozen foundation model within each tile, DI-MIL converts a single tile into multiple independently weighted instance embeddings. As a training-free post-encoding module, DI-MIL integrates seamlessly into existing pipelines without requiring re-encoding or downstream architectural modifications. We evaluate DI-MIL on cytopathology, a challenging testbed where sparse diagnostic signals are easily diluted within standard tiles. Across four datasets, three frozen foundation models, and two attention-based aggregators, DI-MIL demonstrates consistent efficacy, improving 67 of 72 metric-level comparisons, with the largest mean gains reaching 3.64 points under cytopathology-specific backbones. In a broader comparison against seven representative MIL baselines, DI-MIL paired with ACMIL achieves highest mean performance in 33 of 36 backbone-dataset-metric comparisons. Ablations show that direct smaller tiling inflates the extracted tile count by up to 43.3$\times$ with non-monotonic performance, whereas DI-MIL incurs zero additional image-extraction overhead while achieving the strongest overall results. These results establish instance construction as an orthogonal design dimension in MIL, supporting DI-MIL as a cost-efficient solution under sparse diagnostic evidence.

Computer Vision and Pattern Recognition (cs.CV); Machine Learning (cs.LG)

arXiv:2610.04853 [cs.CV]

(or arXiv:2610.04853v1 [cs.CV] for this version)

https://doi.org/10.48550/arXiv.2610.04853 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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