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Ryoma Bise

Publications and source records attributed to Ryoma Bise.

At least 19 recordsLinked to original sources

Weakly Supervised Instance-Level Gleason Pattern Estimation Using Primary and Secondary Labels

In prostate cancer histopathology, the Gleason Score is determined by the most frequent (Primary) and second most frequent (Secondary) Gleason patterns within a whole-slide image. Although these slide-level labels are routinely available in clinical practice, instance-level Gleason annotations are rarely provided, making patch-level learning challenging. We propose a Multiple Instance Learning (MIL) framework that estimates instance-level Gleason patterns from slide-level Primary and Secondary labels. The proposed method formulates instance-level learning according to the clinical definition of the Gleason Score by aggregating instance predictions into class counts and explicitly modeling the Primary pattern, Secondary pattern, and their dominance. Experimental results demonstrate that the proposed formulation enables effective instance-level learning and outperforms existing MIL approaches on the SICAP-MIL dataset.

cs.CV

GC-MoE: Genomics-Guided Cell-Type-Specific Mixture of Experts for Histology-Based Single-Cell Spatial Transcriptomics

Histology-based single-cell spatial transcriptomics (ST) estimation aims to predict gene expression for individual cells from histopathological images and cell locations, reducing the need for costly single-cell ST measurements. Unlike existing histology-to-ST methods that mainly predict spot-level profiles for local regions containing multiple cells, this task requires modeling cell-to-cell expression variability, which is strongly structured by cell type. We propose Genomics-Guided Cell-Type-Specific Mixture-of-Experts (GC-MoE), which estimates cell-type probabilities with a routing network and softly combines cell-type-specific experts for gene expression prediction. To further encode cell-type-dependent gene programs, we introduce the Cell-Type-Specific Co-Expression-Aware Predictor (CAP), together with a lightweight Cell-to-Cell Interaction Attention (C2CA) module for neighboring-cell context. Experiments and ablations on public single-cell ST datasets show consistent improvements over existing single-cell and adapted spot-level baselines.

cs.CV

Leveraging Vision-Language Models as Weak Annotators in Active Learning

Active learning aims to reduce annotation cost by selectively querying informative samples for supervision under a limited labeling budget. In this work, we investigate how vision-language models (VLMs) can be leveraged to further reduce the reliance on costly human annotation within the active learning paradigm. To this end, we find that the reliability of VLMs varies significantly with label granularity in fine-grained recognition tasks: they perform poorly on fine-grained labels but can provide accurate coarse-grained labels. Leveraging this property, we propose an active learning framework that combines fine-grained human annotations with coarse-grained VLM-generated weak labels through instance-wise label assignment. We further model the systematic noise in VLM-generated labels using a small set of trusted full labels. Experiments on CUB200 and FGVC-Aircraft show that the proposed framework consistently outperforms existing active learning methods under the same annotation budget.

cs.CV

Leveraging Spatial Transcriptomics as Alternative to Manual Annotations for Deep Learning-Based Nuclei Analysis

Deep learning-based nuclei segmentation and classification in pathology images typically rely on large-scale pixel-level manual annotations, which are costly and difficult to obtain across diverse tissues and staining conditions. To address this limitation, we propose a framework that leverages spatial transcriptomics (ST) data as supervision for nuclei segmentation and classification. By incorporating cell-level ST data, we obtain gene expression profiles and corresponding nuclear masks from histopathological images. Gene expression profiles are converted into cell-type labels and used as training data for image-based classification. Because existing gene expression-based cell-type classification methods are not designed for image recognition, we introduce an image-oriented classification approach that bridges gene expression-based cell typing and image-based cell classification. To evaluate generalization, we conduct segmentation experiments on previously unseen organs and compare our method with conventional supervised models. Despite being trained on fewer organ types, our framework achieves higher segmentation accuracy, demonstrating strong transferability. Classification experiments further show consistent improvements over existing approaches.

cs.CV

Cell Instance Segmentation via Multi-Task Image-to-Image Schrödinger Bridge

Existing cell instance segmentation pipelines typically combine deterministic predictions with post-processing, which imposes limited explicit constraints on the global structure of instance masks. In this work, we propose a multi-task image-to-image Schrödinger Bridge framework that formulates instance segmentation as a distribution-based image-to-image generation problem. Boundary-aware supervision is integrated through a reverse distance map, and deterministic inference is employed to produce stable predictions. Experimental results on the PanNuke dataset demonstrate that the proposed method achieves competitive or superior performance without relying on SAM pre-training or additional post-processing. Additional results on the MoNuSeg dataset show robustness under limited training data. These findings indicate that Schrödinger Bridge-based image-to-image generation provides an effective framework for cell instance segmentation.

cs.CV

Ranking-Guided Semi-Supervised Domain Adaptation for Severity Classification

Semi-supervised domain adaptation leverages a few labeled and many unlabeled target samples, making it promising for addressing domain shifts in medical image analysis. However, existing methods struggle with severity classification due to unclear class boundaries. Severity classification involves naturally ordered class labels, complicating adaptation. We propose a novel method that aligns source and target domains using rank scores learned via ranking with class order. Specifically, Cross-Domain Ranking ranks sample pairs across domains, while Continuous Distribution Alignment aligns rank score distributions. Experiments on ulcerative colitis and diabetic retinopathy classification validate the effectiveness of our approach, demonstrating successful alignment of class-specific rank score distributions.

cs.CV

Cell-Type Prototype-Informed Neural Network for Gene Expression Estimation from Pathology Images

Estimating slide- and patch-level gene expression profiles from pathology images enables rapid and low-cost molecular analysis with broad clinical impact. Despite strong results, existing approaches treat gene expression as a mere slide- or spot-level signal and do not incorporate the fact that the measured expression arises from the aggregation of underlying cell-level expression. To explicitly introduce this missing cell-resolved guidance, we propose a Cell-type Prototype-informed Neural Network (CPNN) that leverages publicly available single-cell RNA-sequencing datasets. Since single-cell measurements are noisy and not paired with histology images, we first estimate cell-type prototypes-mean expression profiles that reflect stable gene-gene co-variation patterns.CPNN then learns cell-type compositional weights directly from images and models the relationship between prototypes and observed bulk or spatial expression, providing a biologically grounded and structurally regularized prediction framework. We evaluate CPNN on three slide-level datasets and three patch-level spatial transcriptomics datasets. Across all settings, CPNN achieves the highest performance in terms of Spearman correlation. Moreover, by visualizing the inferred compositional weights, our framework provides interpretable insights into which cell types drive the predicted expression. Code is publicly available at https://github.com/naivete5656/CPNN.

cs.CV

VesselFusion: Diffusion Models for Vessel Centerline Extraction from 3D CT Images

Vessel centerline extraction from 3D CT images is an important task because it reduces annotation effort to build a model that estimates a vessel structure. It is challenging to estimate natural vessel structures since conventional approaches are deterministic models, which cannot capture a complex human structure. In this study, we propose VesselFusion, which is a diffusion model to extract the vessel centerline from 3D CT image. The proposed method uses a coarse-to-fine representation of the centerline and a voting-based aggregation for a natural and stable extraction. VesselFusion was evaluated on a publicly available CT image dataset and achieved higher extraction accuracy and a more natural result than conventional approaches.

cs.CV

Leveraging Label Proportion Prior for Class-Imbalanced Semi-Supervised Learning

Semi-supervised learning (SSL) often suffers under class imbalance, where pseudo-labeling amplifies majority bias and suppresses minority performance. We address this issue with a lightweight framework that, to our knowledge, is the first to introduce Proportion Loss from learning from label proportions (LLP) into SSL as a regularization term. Proportion Loss aligns model predictions with the global class distribution, mitigating bias across both majority and minority classes. To further stabilize training, we formulate a stochastic variant that accounts for fluctuations in mini-batch composition. Experiments on the Long-tailed CIFAR-10 benchmark show that integrating Proportion Loss into FixMatch and ReMixMatch consistently improves performance over the baselines across imbalance severities and label ratios, and achieves competitive or superior results compared to existing CISSL methods, particularly under scarce-label conditions.

cs.LG

Hypernetwork-Based Adaptive Aggregation for Multimodal Multiple-Instance Learning in Predicting Coronary Calcium Debulking

In this paper, we present the first attempt to estimate the necessity of debulking coronary artery calcifications from computed tomography (CT) images. We formulate this task as a Multiple-instance Learning (MIL) problem. The difficulty of this task lies in that physicians adjust their focus and decision criteria for device usage according to tabular data representing each patient's condition. To address this issue, we propose a hypernetwork-based adaptive aggregation transformer (HyperAdAgFormer), which adaptively modifies the feature aggregation strategy for each patient based on tabular data through a hypernetwork. The experiments using the clinical dataset demonstrated the effectiveness of HyperAdAgFormer. The code is publicly available at https://github.com/Shiku-Kaito/HyperAdAgFormer.

cs.CV

Learning Relative Gene Expression Trends from Pathology Images in Spatial Transcriptomics

Gene expression estimation from pathology images has the potential to reduce the RNA sequencing cost. Point-wise loss functions have been widely used to minimize the discrepancy between predicted and absolute gene expression values. However, due to the complexity of the sequencing techniques and intrinsic variability across cells, the observed gene expression contains stochastic noise and batch effects, and estimating the absolute expression values accurately remains a significant challenge. To mitigate this, we propose a novel objective of learning relative expression patterns rather than absolute levels. We assume that the relative expression levels of genes exhibit consistent patterns across independent experiments, even when absolute expression values are affected by batch effects and stochastic noise in tissue samples. Based on the assumption, we model the relation and propose a novel loss function called STRank that is robust to noise and batch effects. Experiments using synthetic datasets and real datasets demonstrate the effectiveness of the proposed method. The code is available at https://github.com/naivete5656/STRank.

cs.CV

Auxiliary Gene Learning: Spatial Gene Expression Estimation by Auxiliary Gene Selection

Spatial transcriptomics (ST) is a novel technology that enables the observation of gene expression at the resolution of individual spots within pathological tissues. ST quantifies the expression of tens of thousands of genes in a tissue section; however, heavy observational noise is often introduced during measurement. In prior studies, to ensure meaningful assessment, both training and evaluation have been restricted to only a small subset of highly variable genes, and genes outside this subset have also been excluded from the training process. However, since there are likely co-expression relationships between genes, low-expression genes may still contribute to the estimation of the evaluation target. In this paper, we propose $Auxiliary \ Gene \ Learning$ (AGL) that utilizes the benefit of the ignored genes by reformulating their expression estimation as auxiliary tasks and training them jointly with the primary tasks. To effectively leverage auxiliary genes, we must select a subset of auxiliary genes that positively influence the prediction of the target genes. However, this is a challenging optimization problem due to the vast number of possible combinations. To overcome this challenge, we propose Prior-Knowledge-Based Differentiable Top-$k$ Gene Selection via Bi-level Optimization (DkGSB), a method that ranks genes by leveraging prior knowledge and relaxes the combinatorial selection problem into a differentiable top-$k$ selection problem. The experiments confirm the effectiveness of incorporating auxiliary genes and show that the proposed method outperforms conventional auxiliary task learning approaches.

cs.LG

Domain Adaptation for Ulcerative Colitis Severity Estimation Using Patient-Level Diagnoses

The development of methods to estimate the severity of Ulcerative Colitis (UC) is of significant importance. However, these methods often suffer from domain shifts caused by differences in imaging devices and clinical settings across hospitals. Although several domain adaptation methods have been proposed to address domain shift, they still struggle with the lack of supervision in the target domain or the high cost of annotation. To overcome these challenges, we propose a novel Weakly Supervised Domain Adaptation method that leverages patient-level diagnostic results, which are routinely recorded in UC diagnosis, as weak supervision in the target domain. The proposed method aligns class-wise distributions across domains using Shared Aggregation Tokens and a Max-Severity Triplet Loss, which leverages the characteristic that patient-level diagnoses are determined by the most severe region within each patient. Experimental results demonstrate that our method outperforms comparative DA approaches, improving UC severity estimation in a domain-shifted setting.

cs.CV

Learning from Majority Label: A Novel Problem in Multi-class Multiple-Instance Learning

The paper proposes a novel multi-class Multiple-Instance Learning (MIL) problem called Learning from Majority Label (LML). In LML, the majority class of instances in a bag is assigned as the bag-level label. The goal of LML is to train a classification model that estimates the class of each instance using the majority label. This problem is valuable in a variety of applications, including pathology image segmentation, political voting prediction, customer sentiment analysis, and environmental monitoring. To solve LML, we propose a Counting Network trained to produce bag-level majority labels, estimated by counting the number of instances in each class. Furthermore, analysis experiments on the characteristics of LML revealed that bags with a high proportion of the majority class facilitate learning. Based on this result, we developed a Majority Proportion Enhancement Module (MPEM) that increases the proportion of the majority class by removing minority class instances within the bags. Experiments demonstrate the superiority of the proposed method on four datasets compared to conventional MIL methods. Moreover, ablation studies confirmed the effectiveness of each module. The code is available at \href{https://github.com/Shiku-Kaito/Learning-from-Majority-Label-A-Novel-Problem-in-Multi-class-Multiple-Instance-Learning}{here}.

cs.CV

NoiseCutMix: A Novel Data Augmentation Approach by Mixing Estimated Noise in Diffusion Models

In this study, we propose a novel data augmentation method that introduces the concept of CutMix into the generation process of diffusion models, thereby exploiting both the ability of diffusion models to generate natural and high-resolution images and the characteristic of CutMix, which combines features from two classes to create diverse augmented data. Representative data augmentation methods for combining images from multiple classes include CutMix and MixUp. However, techniques like CutMix often result in unnatural boundaries between the two images due to contextual differences. Therefore, in this study, we propose a method, called NoiseCutMix, to achieve natural, high-resolution image generation featuring the fused characteristics of two classes by partially combining the estimated noise corresponding to two different classes in a diffusion model. In the classification experiments, we verified the effectiveness of the proposed method by comparing it with conventional data augmentation techniques that combine multiple classes, random image generation using Stable Diffusion, and combinations of these methods. Our codes are available at: https://github.com/shumpei-takezaki/NoiseCutMix

cs.CV

Enhancing Reliability of Medical Image Diagnosis through Top-rank Learning with Rejection Module

In medical image processing, accurate diagnosis is of paramount importance. Leveraging machine learning techniques, particularly top-rank learning, shows significant promise by focusing on the most crucial instances. However, challenges arise from noisy labels and class-ambiguous instances, which can severely hinder the top-rank objective, as they may be erroneously placed among the top-ranked instances. To address these, we propose a novel approach that enhances toprank learning by integrating a rejection module. Cooptimized with the top-rank loss, this module identifies and mitigates the impact of outliers that hinder training effectiveness. The rejection module functions as an additional branch, assessing instances based on a rejection function that measures their deviation from the norm. Through experimental validation on a medical dataset, our methodology demonstrates its efficacy in detecting and mitigating outliers, improving the reliability and accuracy of medical image diagnoses.

cs.CV

Domain Generalization of Pathological Image Segmentation by Patch-Level and WSI-Level Contrastive Learning

In this paper, we address domain shifts in pathological images by focusing on shifts within whole slide images~(WSIs), such as patient characteristics and tissue thickness, rather than shifts between hospitals. Traditional approaches rely on multi-hospital data, but data collection challenges often make this impractical. Therefore, the proposed domain generalization method captures and leverages intra-hospital domain shifts by clustering WSI-level features from non-tumor regions and treating these clusters as domains. To mitigate domain shift, we apply contrastive learning to reduce feature gaps between WSI pairs from different clusters. The proposed method introduces a two-stage contrastive learning approach WSI-level and patch-level contrastive learning to minimize these gaps effectively.

cs.CV

Adaptive Pseudo Label Selection for Individual Unlabeled Data by Positive and Unlabeled Learning

This paper proposes a novel pseudo-labeling method for medical image segmentation that can perform learning on ``individual images'' to select effective pseudo-labels. We introduce Positive and Unlabeled Learning (PU learning), which uses only positive and unlabeled data for binary classification problems, to obtain the appropriate metric for discriminating foreground and background regions on each unlabeled image. Our PU learning makes us easy to select pseudo-labels for various background regions. The experimental results show the effectiveness of our method.

cs.CV