Current deep learning approaches for lithium-ion battery analysis are often specialized and limited to specific battery types or individual tasks. While recent advances in large language models (LLMs) highlight the potential of pretraining paradigms, existing time-series pretraining models inadequately address the physicochemical complexity and temporal irregularity inherent to battery operational data. We propose LiPM, a pretrained foundation model that unifies multi-dataset learning through physics-aware objectives and irregularity-tolerant temporal modeling. LiPM introduces three key innovations: (1) A Mix-Masked Autoencoder (MMAE) enforcing electrochemical consistency via joint reconstruction of temporally masked patches and cross-channel masked variables(2) A Coulombic Integration Regression (CIR) task explicitly encoding charge conservation laws, and (3) A dual-scale temporal encoder combining irregular intra-patch processing (preserving raw timestamps) with regular inter-patch attention (capturing macroscopic dynamics). Trained on eight heterogeneous battery datasets without cycle-label annotations, LiPM demonstrates universal applicability across partial charge-discharge segments and irregular sampling protocols. Extensive experiments show remarkable improvements over 9 state-of-the-art baselines in critical downstream tasks.

Pathogenic chromosome abnormalities are very common among the general population. While numerical chromosome abnormalities can be quickly and precisely detected, structural chromosome abnormalities are far more complex and typically require considerable efforts by human experts for identification. This paper focuses on investigating the modeling of chromosome features and the identification of chromosomes with structural abnormalities. Most existing data-driven methods concentrate on a single chromosome and consider each chromosome independently, overlooking the crucial aspect of homologous chromosomes. In normal cases, homologous chromosomes share identical structures, with the exception that one of them is abnormal. Therefore, we propose an adaptive method to align homologous chromosomes and diagnose structural abnormalities through homologous similarity. Inspired by the process of human expert diagnosis, we incorporate information from multiple pairs of homologous chromosomes simultaneously, aiming to reduce noise disturbance and improve prediction performance. Extensive experiments on real-world datasets validate the effectiveness of our model compared to baselines.

A taocode is a kind of specially coded text-link on taobao.com (the world's biggest online shopping website), through which users can share messages about products with each other. Analyzing taocodes can potentially facilitate understanding of the social relationships between users and, more excitingly, their online purchasing behaviors under the influence of taocode diffusion. This paper innovatively investigates the problem of online purchasing predictions from an information diffusion perspective, with taocode as a case study. Specifically, we conduct profound observational studies on a large-scale real-world dataset from Taobao, containing over 100M Taocode sharing records. Inspired by our observations, we propose InfNet, a dynamic GNN-based framework that models the information diffusion across Taocode. We then apply InfNet to item purchasing predictions. Extensive experiments on real-world datasets validate the effectiveness of InfNet compared with νmofbaseline~ state-of-the-art baselines.