Kaito Shiku

Kaito Shiku, Ahtisham Fazeel Abbasi, Ryoma Bise et al.

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.

Kazuya Nishimura, Haruka Hirose, Ryoma Bise et al.

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.

Kaito Shiku, Ichika Seo, Tetsuya Matoba et al.

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.

Phuong Ngoc Nguyen, Kaito Shiku, Ryoma Bise et al.

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.

Kaito Shiku, Kazuya Nishimura, Daiki Suehiro et al.

Patient-level diagnosis of severity in ulcerative colitis (UC) is common in real clinical settings, where the most severe score in a patient is recorded. However, previous UC classification methods (i.e., image-level estimation) mainly assumed the input was a single image. Thus, these methods can not utilize severity labels recorded in real clinical settings. In this paper, we propose a patient-level severity estimation method by a transformer with selective aggregator tokens, where a severity label is estimated from multiple images taken from a patient, similar to a clinical setting. Our method can effectively aggregate features of severe parts from a set of images captured in each patient, and it facilitates improving the discriminative ability between adjacent severity classes. Experiments demonstrate the effectiveness of the proposed method on two datasets compared with the state-of-the-art MIL methods. Moreover, we evaluated our method in real clinical settings and confirmed that our method outperformed the previous image-level methods. The code is publicly available at https://github.com/Shiku-Kaito/Ordinal-Multiple-instance-Learning-for-Ulcerative-Colitis-Severity-Estimation.

Kaito Shiku, Shinnosuke Matsuo, Daiki Suehiro et al.

The paper proposes a novel problem in multi-class Multiple-Instance Learning (MIL) called Learning from the Majority Label (LML). In LML, the majority class of instances in a bag is assigned as the bag's label. LML aims to classify instances using bag-level majority classes. This problem is valuable in various applications. Existing MIL methods are unsuitable for LML due to aggregating confidences, which may lead to inconsistency between the bag-level label and the label obtained by counting the number of instances for each class. This may lead to incorrect instance-level classification. We propose a counting network trained to produce the bag-level majority labels estimated by counting the number of instances for each class. This led to the consistency of the majority class between the network outputs and one obtained by counting the number of instances. Experimental results show that our counting network outperforms conventional MIL methods on four datasets The code is publicly available at https://github.com/Shiku-Kaito/Counting-Network-for-Learning-from-Majority-Label.

Yugo Kubota, Kaito Shiku, Seiichi Uchida

Font shapes can evoke a wide range of impressions, but the correspondence between fonts and impression descriptions is not one-to-one: some impressions are broadly compatible with diverse styles, whereas others strongly constrain the set of plausible fonts. We refer to this graded constraint strength as style specificity. In this paper, we propose a hyperbolic co-embedding framework that models font--impression correspondence through entailment rather than simple paired alignment. Font images and impression descriptions, represented as single tags or tag sets, are embedded in a shared hyperbolic space with two complementary entailment constraints: impression-to-font entailment and low-to-high style-specificity entailment among impressions. This formulation induces a radial structure in which low style-specificity impressions lie near the origin and high style-specificity impressions lie farther away, yielding an interpretable geometric measure of how strongly an impression constrains font style. Experiments on the MyFonts dataset demonstrate improved bidirectional retrieval over strong one-to-one baselines. In addition, traversal and tag-level analyses show that the learned space captures a coherent progression from ambiguous to more style-specific impressions and provides a meaningful, data-driven quantification of style specificity.

Kaito Shiku, Kazuya Nishimura, Shinnosuke Matsuo et al.

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.

Takamasa Yamaguchi, Brian Kenji Iwana, Ryoma Bise et al.

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.

Kaito Shiku, Hiromitsu Shirai, Takeshi Ishihara et al.

3D cell tracking in a living organism has a crucial role in live cell image analysis. Cell tracking in C. elegans has two difficulties. First, cell migration in a consecutive frame is large since they move their head during scanning. Second, cell detection is often inconsistent in consecutive frames due to touching cells and low-contrast images, and these inconsistent detections affect the tracking performance worse. In this paper, we propose a cell tracking method to address these issues, which has two main contributions. First, we introduce cell position heatmap-based non-rigid alignment with test-time fine-tuning, which can warp the detected points to near the positions at the next frame. Second, we propose a pairwise detection method, which uses the information of detection results at the previous frame for detecting cells at the current frame. The experimental results demonstrate the effectiveness of each module, and the proposed method achieved the best performance in comparison.