#01Nov 12, 2026
cs.CV
FLEX-LBP: Learning Local Binary Patterns with Exact Binary Inference for Texture Classification
Mohamed Alimoussa, Amal El Kaid
Local Binary Patterns (LBP) remain among the most widely used texture descriptors, from industrial inspection to medical imaging. Yet their radius, sampling angles, color transform and thresholds are fixed by hand for each dataset. We present FLEX-LBP, which learns these parameters by backpropagation while every forward pass computes exact binary codes and hard histogram counts. A straight-through estimator acts only in the backward pass, so the deployed descriptor is an interpretable hard-binary LBP with 90 learnable parameters and unchanged inference cost. In a controlled ablation on six color texture benchmarks, the component worth learning is dataset-dependent. One configuration, applied unchanged everywhere, learns the geometry and thresholds with the color transform frozen. It improves the nearest-neighbor accuracy of the identical fixed descriptor by 3.55 points on average over five seeds, significantly on five of six benchmarks and never significantly worse. With a linear discriminant readout, it gains 0.9 points; the fully learned descriptor gains 2.7 and has the highest mean. FLEX-LBP is more accurate than five classical LBP-family descriptors, PCANet and a neural LBP on five of six benchmarks. Its mean nearest-neighbor accuracy exceeds that of frozen ImageNet ResNet-50 features (23.5 million parameters). On the Kather colorectal cancer histology benchmark, the fully learned descriptor reaches 93.8%, significantly above the best classical descriptor (Completed LBP, 92.8%). The learned radii adapt in directions that recur across seeds. Noise drowns single-pixel comparisons and illuminant change flips inter-channel ones; median sampling or gray-world normalization restores 96-97%. The code is available as a drop-in PyTorch layer at https://github.com/medalimoussa/FLEX-LBP.
#02Nov 12, 2026
cs.CV
TuMAP: A Dual-View, Morphotype-Aware Pathomics Pipeline for Quantifying Renal Tubular Remodeling
Ruijie Wu, Yuechen Yang, Yanfan Zhu and 8 more
Quantifying disease-associated renal tubular remodeling is challenging because tubular appearances are heterogeneous. We introduce TuMAP (Tubular Morphotype-Aware Pathomics), a pipeline combining (1) dual-view foundation-model representations and provisional morphotype annotation, (2) compositional and within-morphotype pathomics, and (3) patient-level statistical inference. From 456,158 tubules in 358 PAS-stained kidney biopsy slides, TuMAP identified eight image-based morphotypes, seven of which showed stable subsampling assignments. Across 219 patients in six diagnostic groups, diabetic nephropathy (DN) and tubulointerstitial nephritis/acute tubular injury (TIN/ATI) each differed from minimal change disease in seven morphotype proportions, while IgA nephropathy differed in six. DN showed reduced nuclear solidity and increased eccentricity across all eight morphotypes. Area-normalized nuclear density exposed additional within-morphotype differences. TuMAP provides a framework for separating changes in tubular morphotype composition from phenotypic differences within morphotypes.
#03Nov 12, 2026
cs.CV
Joint Null-Space Projection for Data-Free Model Merging
Tian Xia
Merging independently fine-tuned checkpoints into a single multi-task model requires no data, no labels, and no gradient steps. In practice the task vectors of different tasks interfere, and the standard remedies--averaging, magnitude pruning, sign election--operate entry by entry, ignoring that each delta induces a low-dimensional update on the hidden features it acts upon. We recast merging as a subspace interference problem. For every two-dimensional weight tensor we take the top-r right-singular subspace of each task's delta--the input directions along which that task moves the representation most--and remove from each task vector the component lying in the union of the other tasks' subspaces. The resulting Joint Null-Space Projection (JNSP) is closed-form and order-independent, needs no forward pass, and is defined entirely by the checkpoint set. On eight CLIP image-classification tasks JNSP merges ViT-B/16 experts to 89.45% average accuracy without using a single image, 11.88 points above the strongest parameter-wise training-free baseline (TIES-Merging, 77.57%), 14.22 above Task Arithmetic, and 0.98 above WUDI's data-free consensus merge (88.47%). The gain holds across three backbones on the independently trained TALL release (+10.8, +12.6, +9.1 over TIES for ViT-B/16, ViT-B/32, ViT-L/14) and replicates there at 89.20%; controls confirm the source--a single shared subspace instead of per-task ones loses 2.9 points, and a sequential variant collapses to 69.6%. On RoBERTa-large the same projection underperforms plain task arithmetic, which we report rather than hide. Code is available at https://github.com.
#04Nov 12, 2026
cs.CV
eDMD: Endpoint Distribution Matching for Few-Step Diffusion Distillation
Tong Zhao, Xianfang Zeng, Yucheng Han and 4 more
Distribution matching distillation (DMD) has emerged as a leading paradigm for distilling diffusion models into few-step students, where an auxiliary fake score model tracks the student's distribution and the discrepancy between the teacher and fake predictions drives the student toward the teacher. In multi-step distillation, although only the student's final output is delivered, existing methods train the fake model on intermediate states or across all denoising steps. Consequently, the student's update signal becomes entangled with intermediate distributions, which can distort the matching direction and remain nonzero even after the student's final outputs already match the teacher distribution. To resolve this mismatch, we propose Endpoint Distribution Matching Distillation (eDMD), which trains a single shared fake model exclusively on the student's final outputs and uses it to correct every denoising step. Our theoretical analysis proves that this endpoint reference guarantees that the distribution matching term vanishes if and only if the student's final output distribution matches the teacher's, regardless of intermediate distributions. Beyond the fake reference, we further strengthen teacher supervision through a precise teacher (PT) that replaces single-step guided predictions with short multi-step trajectories on the final noise interval, paired with a calibrated query density for intermediate steps. Experiments on SD3-Medium, FLUX.2-klein (4B and 9B), and Qwen-Image-2.1 demonstrate that eDMD consistently outperforms existing distribution matching methods for 4-step generation.
#05Nov 12, 2026
cs.CV
Predicting Ethanol Drinking Status from Nonhuman Primate Liver Histology: A Proof of Concept for Parameter-efficient Fine-tuning in Few-Shot Vision-Language Modeling
Amirmohammad Mohammadi, Rupak Khadka, Kathleen A. Grant and 2 more
Combining vision-language models (VLMs) with parameter-efficient fine-tuning (PEFT) offers a promising approach to few-shot whole-slide image (WSI) classification in computational pathology. This study evaluates this approach for predicting ethanol drinking status from nonhuman primate liver histology. Adapters are evaluated against non-PEFT configurations on a subset of the Monkey Alcohol Tissue Research Resource (MATRR). All evaluated PEFT configurations achieve higher mean balanced accuracy than the non-PEFT baselines. For example, in the four-shot setting, attention-based multiple instance learning (ABMIL) alone achieves 43.5% mean balanced accuracy, compared with 78.1% after adding an adapter. Qualitative attention analysis shows that textual pathway adaptations produce localized attention heatmaps, while visual pathway adaptations produce more diffuse ones. A pathologist's review identified similar histological features across adaptations.