Pengjiang Li

Le Ma, Ran Zhang, Yikun Han et al.

Vector databases (VDBs) have emerged to manage high-dimensional data that exceed the capabilities of traditional database management systems, and are now tightly integrated with large language models as well as widely applied in modern artificial intelligence systems. Although relatively few studies describe existing or introduce new vector database architectures, the core technologies underlying VDBs, such as approximate nearest neighbor search, have been extensively studied and are well documented in the literature. In this work, we present a comprehensive review of the relevant algorithms to provide a general understanding of this booming research area. Specifically, we first provide a review of storage and retrieval techniques in VDBs, with detailed design principles and technological evolution. Then, we conduct an in-depth comparison of several advanced VDB solutions with their strengths, limitations, and typical application scenarios. Finally, we also outline emerging opportunities for coupling VDBs with large language models, including open research problems and trends, such as novel indexing strategies. This survey aims to serve as a practical resource, enabling readers to quickly gain an overall understanding of the current knowledge landscape in this rapidly developing area.

Ping Xu, Zaitian Wang, Zhirui Wang et al.

Cell clustering is crucial for uncovering cellular heterogeneity in single-cell RNA sequencing (scRNA-seq) data by identifying cell types and marker genes. Despite its importance, benchmarks for scRNA-seq clustering methods remain fragmented, often lacking standardized protocols and failing to incorporate recent advances in artificial intelligence. To fill these gaps, we present scCluBench, a comprehensive benchmark of clustering algorithms for scRNA-seq data. First, scCluBench provides 36 scRNA-seq datasets collected from diverse public sources, covering multiple tissues, which are uniformly processed and standardized to ensure consistency for systematic evaluation and downstream analyses. To evaluate performance, we collect and reproduce a range of scRNA-seq clustering methods, including traditional, deep learning-based, graph-based, and biological foundation models. We comprehensively evaluate each method both quantitatively and qualitatively, using core performance metrics as well as visualization analyses. Furthermore, we construct representative downstream biological tasks, such as marker gene identification and cell type annotation, to further assess the practical utility. scCluBench then investigates the performance differences and applicability boundaries of various clustering models across diverse analytical tasks, systematically assessing their robustness and scalability in real-world scenarios. Overall, scCluBench offers a standardized and user-friendly benchmark for scRNA-seq clustering, with curated datasets, unified evaluation protocols, and transparent analyses, facilitating informed method selection and providing valuable insights into model generalizability and application scope.

Ping Xu, Zhiyuan Ning, Pengjiang Li et al.

Single-cell RNA sequencing (scRNA-seq) reveals cell heterogeneity, with cell clustering playing a key role in identifying cell types and marker genes. Recent advances, especially graph neural networks (GNNs)-based methods, have significantly improved clustering performance. However, the analysis of scRNA-seq data remains challenging due to noise, sparsity, and high dimensionality. Compounding these challenges, GNNs often suffer from over-smoothing, limiting their ability to capture complex biological information. In response, we propose scSiameseClu, a novel Siamese Clustering framework for interpreting single-cell RNA-seq data, comprising of 3 key steps: (1) Dual Augmentation Module, which applies biologically informed perturbations to the gene expression matrix and cell graph relationships to enhance representation robustness; (2) Siamese Fusion Module, which combines cross-correlation refinement and adaptive information fusion to capture complex cellular relationships while mitigating over-smoothing; and (3) Optimal Transport Clustering, which utilizes Sinkhorn distance to efficiently align cluster assignments with predefined proportions while maintaining balance. Comprehensive evaluations on seven real-world datasets demonstrate that scSiameseClu outperforms state-of-the-art methods in single-cell clustering, cell type annotation, and cell type classification, providing a powerful tool for scRNA-seq data interpretation.

Ping Xu, Zaitian Wang, Zhirui Wang et al.

Single-cell RNA sequencing (scRNA-seq) technology enables systematic delineation of cellular states and interactions, providing crucial insights into cellular heterogeneity. Building on this potential, numerous computational methods have been developed for tasks such as cell clustering, cell type annotation, and marker gene identification. To fully assess and compare these methods, standardized, analysis-ready datasets are essential. However, such datasets remain scarce, and variations in data formats, preprocessing workflows, and annotation strategies hinder reproducibility and complicate systematic evaluation of existing methods. To address these challenges, we present scUnified, an AI-ready standardized resource for single-cell RNA sequencing data that consolidates 13 high-quality datasets spanning two species (human and mouse) and nine tissue types. All datasets undergo standardized quality control and preprocessing and are stored in a uniform format to enable direct application in diverse computational analyses without additional data cleaning. We further demonstrate the utility of scUnified through experimental analyses of representative biological tasks, providing a reproducible foundation for the standardized evaluation of computational methods on a unified dataset.

Pengjiang Li, Zaitian Wang, Xinhao Zhang et al.

Topic discovery in scientific literature provides valuable insights for researchers to identify emerging trends and explore new avenues for investigation, facilitating easier scientific information retrieval. Many machine learning methods, particularly deep embedding techniques, have been applied to discover research topics. However, most existing topic discovery methods rely on word embedding to capture the semantics and lack a comprehensive understanding of scientific publications, struggling with complex, high-dimensional text relationships. Inspired by the exceptional comprehension of textual information by large language models (LLMs), we propose an advanced topic discovery method enhanced by LLMs to improve scientific topic identification, namely SciTopic. Specifically, we first build a textual encoder to capture the content from scientific publications, including metadata, title, and abstract. Next, we construct a space optimization module that integrates entropy-based sampling and triplet tasks guided by LLMs, enhancing the focus on thematic relevance and contextual intricacies between ambiguous instances. Then, we propose to fine-tune the textual encoder based on the guidance from the LLMs by optimizing the contrastive loss of the triplets, forcing the text encoder to better discriminate instances of different topics. Finally, extensive experiments conducted on three real-world datasets of scientific publications demonstrate that SciTopic outperforms the state-of-the-art (SOTA) scientific topic discovery methods, enabling researchers to gain deeper and faster insights.