Yuichiro Iwashita

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.

Shaonan Liu, Yuichiro Iwashita, Soichiro Nakako et al.

Electronic health records (EHRs) are invaluable for clinical research, yet privacy concerns severely restrict data sharing. Synthetic data generation offers a promising solution, but EHRs present unique challenges: they contain both numerical and categorical features that evolve over time. While diffusion models have demonstrated strong performance in EHR synthesis, existing approaches predominantly rely on discrete-time formulations, which suffer from finite-step approximation errors and coupled training-sampling step counts. We propose a continuous-time diffusion framework for generating mixed-type time-series EHRs with three contributions: (1) continuous-time diffusion with a bidirectional gated recurrent unit backbone for capturing temporal dependencies, (2) unified Gaussian diffusion via learnable continuous embeddings for categorical variables, enabling joint cross-feature modeling, and (3) a factorized learnable noise schedule that adapts to per-feature-per-timestep learning difficulties. Experiments on two large-scale intensive care unit datasets demonstrate that our method outperforms existing approaches in downstream task performance, distribution fidelity, and discriminability, while requiring only 50 sampling steps compared to 1,000 for baseline methods. Classifier-free guidance further enables effective conditional generation for class-imbalanced clinical scenarios.

Yuichiro Iwashita, Ahtisham Fazeel Abbasi, Muhammad Nabeel Asim et al.

Single-cell RNA sequencing (scRNA-seq) is inherently affected by sparsity caused by dropout events, in which expressed genes are recorded as zeros due to technical limitations. These artifacts distort gene expression distributions and can compromise downstream analyses. Numerous imputation methods have been proposed to address this, and these methods encompass a wide range of approaches from traditional statistical models to recently developed deep learning (DL)-based methods. However, their comparative performance remains unclear, as existing benchmarking studies typically evaluate only a limited subset of methods, datasets, and downstream analytical tasks. Here, we present a comprehensive benchmark of 15 scRNA-seq imputation methods spanning 7 methodological categories, including traditional and modern DL-based methods. These methods are evaluated across 30 datasets sourced from 10 experimental protocols and assessed in terms of 6 downstream analytical tasks. Our results show that traditional imputation methods, such as model-based, smoothing-based, and low-rank matrix-based methods, generally outperform DL-based methods, such as diffusion-based, GAN-based, GNN-based, and autoencoder-based methods. In addition, strong performance in numerical gene expression recovery does not necessarily translate into improved biological interpretability in downstream analyses. Furthermore, the performance of imputation methods varies substantially across datasets, protocols, and downstream analytical tasks, and no single method consistently outperforms others across all evaluation scenarios. Together, our results provide practical guidance for selecting imputation methods tailored to specific analytical objectives and highlight the importance of task-specific evaluation when assessing imputation performance in scRNA-seq data analysis.

David Selby, Kai Spriestersbach, Yuichiro Iwashita et al.

Large language models (LLMs) have been extensively studied for their abilities to generate convincing natural language sequences, however their utility for quantitative information retrieval is less well understood. Here we explore the feasibility of LLMs as a mechanism for quantitative knowledge retrieval to aid two data analysis tasks: elicitation of prior distributions for Bayesian models and imputation of missing data. We introduce a framework that leverages LLMs to enhance Bayesian workflows by eliciting expert-like prior knowledge and imputing missing data. Tested on diverse datasets, this approach can improve predictive accuracy and reduce data requirements, offering significant potential in healthcare, environmental science and engineering applications. We discuss the implications and challenges of treating LLMs as 'experts'.