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SAGE advances generative modeling by disentangling salient factors from frozen autoencoder latents to enable unsupervised subtype discovery and high-fidelity image generation. The method demonstrates significant improvements in reconstruction accuracy and diversity across datasets like eyeglass faces and retinal scans, offering a robust framework for analyzing complex visual substructures without explicit labels.
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SAGE: Salient Factor Discovery and Generation with Visual Foundation Representations

arXiv2 min read

arXiv:2609.39635v1 Announce Type: cross Abstract: Given a target dataset, such as faces with eyeglasses, and a background dataset, such as faces without, contrastive analysis separates \textit{salient} factors specific to the target from \textit{common} content shared by both. We aim for salient representations that capture target-specific detail in each image, such as the shape, color, and position of the glasses, so that they reveal subtypes without subtype labels and guide the generation of new examples of a discovered subtype, even one with no name or text description. We introduce SAGE, which learns both factors directly in the high-dimensional spatial latent of a frozen representation autoencoder and conditions a diffusion transformer on the learned salient representation of a reference image. On Digits-ImageNet and FFHQ eyeglasses, SAGE combines high-fidelity \textit{reconstruction} (rFID below $2$) with unsupervised \textit{subtype discovery}, recovering the digits better than baselines (probe accuracy $0.950$ vs.\ at most $0.281$) and revealing eyewear types, finer sunglasses styles, and mislabeled images; salient-conditioned \textit{generation} raises Digits-ImageNet subtype accuracy over the unfactorized latent ($90.5\%$ vs.\ $27.7\%$) and diversity on both datasets. On retinal OCT, SAGE's salient space separates three diseases using only normal/disease labels.

Abstract:Given a target dataset, such as faces with eyeglasses, and a background dataset, such as faces without, contrastive analysis separates \textit{salient} factors specific to the target from \textit{common} content shared by both. We aim for salient representations that capture target-specific detail in each image, such as the shape, color, and position of the glasses, so that they reveal subtypes without subtype labels and guide the generation of new examples of a discovered subtype, even one with no name or text description. We introduce SAGE, which learns both factors directly in the high-dimensional spatial latent of a frozen representation autoencoder and conditions a diffusion transformer on the learned salient representation of a reference image. On Digits-ImageNet and FFHQ eyeglasses, SAGE combines high-fidelity \textit{reconstruction} (rFID below $2$) with unsupervised \textit{subtype discovery}, recovering the digits better than baselines (probe accuracy $0.950$ vs.\ at most $0.281$) and revealing eyewear types, finer sunglasses styles, and mislabeled images; salient-conditioned \textit{generation} raises Digits-ImageNet subtype accuracy over the unfactorized latent ($90.5\%$ vs.\ $27.7\%$) and diversity on both datasets. On retinal OCT, SAGE's salient space separates three diseases using only normal/disease labels.

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

arXiv:2609.39635 [cs.CV]

(or arXiv:2609.39635v1 [cs.CV] for this version)

https://doi.org/10.48550/arXiv.2609.39635 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 283 words

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