Lizhuang Liu

Kun Wu, Zixu Wang, Xiulong Yang et al.

As the primary mRNA delivery vehicles, ionizable lipid nanoparticles (LNPs) exhibit excellent safety, high transfection efficiency, and strong immune response induction. However, the screening process for LNPs is time-consuming and costly. To expedite the identification of high-transfection-efficiency mRNA drug delivery systems, we propose an explainable LNPs transfection efficiency prediction model, called TransMA. TransMA employs a multi-modal molecular structure fusion architecture, wherein the fine-grained atomic spatial relationship extractor named molecule 3D Transformer captures three-dimensional spatial features of the molecule, and the coarse-grained atomic sequence extractor named molecule Mamba captures one-dimensional molecular features. We design the mol-attention mechanism block, enabling it to align coarse and fine-grained atomic features and captures relationships between atomic spatial and sequential structures. TransMA achieves state-of-the-art performance in predicting transfection efficiency using the scaffold and cliff data splitting methods on the current largest LNPs dataset, including Hela and RAW cell lines. Moreover, we find that TransMA captures the relationship between subtle structural changes and significant transfection efficiency variations, providing valuable insights for LNPs design. Additionally, TransMA's predictions on external transfection efficiency data maintain a consistent order with actual transfection efficiencies, demonstrating its robust generalization capability. The code, model and data are made publicly available at https://github.com/wklix/TransMA/tree/master. We hope that high-accuracy transfection prediction models in the future can aid in LNPs design and initial screening, thereby assisting in accelerating the mRNA design process.

Chengying She, Chengwei Chen, Xinran Zhang et al.

Multimodal evidence is critical in computational pathology: gigapixel whole slide images capture tumor morphology, while patient-level clinical descriptors preserve complementary context for prognosis. Integrating such heterogeneous signals remains challenging because feature spaces exhibit distinct statistics and scales. We introduce MMSF, a multitask and multimodal supervised framework built on a linear-complexity MIL backbone that explicitly decomposes and fuses cross-modal information. MMSF comprises a graph feature extraction module embedding tissue topology at the patch level, a clinical data embedding module standardizing patient attributes, a feature fusion module aligning modality-shared and modality-specific representations, and a Mamba-based MIL encoder with multitask prediction heads. Experiments on CAMELYON16 and TCGA-NSCLC demonstrate 2.1--6.6\% accuracy and 2.2--6.9\% AUC improvements over competitive baselines, while evaluations on five TCGA survival cohorts yield 7.1--9.8\% C-index improvements compared with unimodal methods and 5.6--7.1\% over multimodal alternatives.

Chengying She, Chengwei Chen, Dongjie Fan et al.

Whole slide images (WSIs) classification represents a fundamental challenge in computational pathology, where multiple instance learning (MIL) has emerged as the dominant paradigm. Current state-of-the-art (SOTA) MIL methods rely on attention mechanisms, achieving good performance but requiring substantial computational resources due to quadratic complexity when processing hundreds of thousands of patches. To address this computational bottleneck, we introduce EfficientMIL, a novel linear-complexity MIL approach for WSIs classification with the patches selection module Adaptive Patch Selector (APS) that we designed, replacing the quadratic-complexity self-attention mechanisms in Transformer-based MIL methods with efficient sequence models including RNN-based GRU, LSTM, and State Space Model (SSM) Mamba. EfficientMIL achieves significant computational efficiency improvements while outperforming other MIL methods across multiple histopathology datasets. On TCGA-Lung dataset, EfficientMIL-Mamba achieved AUC of 0.976 and accuracy of 0.933, while on CAMELYON16 dataset, EfficientMIL-GRU achieved AUC of 0.990 and accuracy of 0.975, surpassing previous state-of-the-art methods. Extensive experiments demonstrate that APS is also more effective for patches selection than conventional selection strategies.