Good Papers

SAGE: Salient Factor Discovery and Generation with Visual Foundation Representations

SAGE learns salient factors in frozen autoencoder latents to discover unlabeled subtypes and generate high-fidelity subtype-specific examples.

Shuang Liang, Lejun Liao, Shiyuan Zhang, Max C. Zhang, Xiaolong Luo, Han Wang, Stefano Anzellotti, Yuan Yuan

Published Sep 30, 2026▲ 1 on Hugging FacearXiv ↗

77%
OverallHighly rated
?
OverallHighly ratedVote to see the score
Readers
–

Only vote on papers you've read. Sign in to vote.

AI panel11/20reviewers recommend it
lenient 5/5
medium 4/10
strict 2/5
AI panel?Vote to see what the 20 AI reviewers said

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.