Paper List
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Discovery of a Hematopoietic Manifold in scGPT Yields a Method for Extracting Performant Algorithms from Biological Foundation Model Internals
This work addresses the core challenge of extracting reusable, interpretable, and high-performance biological algorithms from the opaque internal repr...
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MS2MetGAN: Latent-space adversarial training for metabolite–spectrum matching in MS/MS database search
This paper addresses the critical bottleneck in metabolite identification: the generation of high-quality negative training samples that are structura...
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Toward Robust, Reproducible, and Widely Accessible Intracranial Language Brain-Computer Interfaces: A Comprehensive Review of Neural Mechanisms, Hardware, Algorithms, Evaluation, Clinical Pathways and Future Directions
This review addresses the core challenge of fragmented and heterogeneous evidence that hinders the clinical translation of intracranial language BCIs,...
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Less Is More in Chemotherapy of Breast Cancer
通过纳入细胞周期时滞和竞争项,解决了现有肿瘤-免疫模型的过度简化问题,以定量比较化疗方案。
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Fold-CP: A Context Parallelism Framework for Biomolecular Modeling
This paper addresses the critical bottleneck of GPU memory limitations that restrict AlphaFold 3-like models to processing only a few thousand residue...
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Open Biomedical Knowledge Graphs at Scale: Construction, Federation, and AI Agent Access with Samyama Graph Database
This paper addresses the core pain point of fragmented biomedical data by constructing and federating large-scale, open knowledge graphs to enable sea...
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Predictive Analytics for Foot Ulcers Using Time-Series Temperature and Pressure Data
This paper addresses the critical need for continuous, real-time monitoring of diabetic foot health by developing an unsupervised anomaly detection fr...
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Hypothesis-Based Particle Detection for Accurate Nanoparticle Counting and Digital Diagnostics
This paper addresses the core challenge of achieving accurate, interpretable, and training-free nanoparticle counting in digital diagnostic assays, wh...
scCluBench: Comprehensive Benchmarking of Clustering Algorithms for Single-Cell RNA Sequencing
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IN SHORT: This paper addresses the critical gap of fragmented and non-standardized benchmarking in single-cell RNA-seq clustering, which hinders objective comparison and selection of appropriate methods for specific biological contexts.
核心创新
- Methodology Introduces scCluBench, the first comprehensive benchmarking framework that systematically evaluates 16 clustering methods across four categories (traditional, deep learning-based, graph-based, and foundation models) on 36 standardized datasets.
- Methodology Establishes standardized protocols for biological interpretation, including reproducible pipelines for marker gene identification and two distinct cell type annotation approaches (best-mapping and marker-overlap), validated with gold-standard references.
- Methodology Provides a unified and modular benchmarking workflow covering data preprocessing, clustering, and annotation with standardized input-output formats, ensuring reproducibility and fair comparison.
主要结论
- scCDCG (a cut-informed graph embedding model) achieved the highest average clustering accuracy (81.29 ± 1.45) across 36 datasets, outperforming other graph-based, deep learning, and traditional methods.
- Biological foundation models (scGPT, GeneFormer, GeneCompass) showed strong performance in classification tasks (e.g., scGPT achieved 98.14% ACC on Sapiens Ear Crista Ampullaris) but underperformed in direct clustering, highlighting a trade-off between general representation and task-specific optimization.
- The benchmark reveals method-specific limitations: traditional methods struggle with sparse data, deep learning models may fail to capture cell relationships, and graph-based models can suffer from over-smoothing, while most methods decouple embedding learning from clustering optimization.
摘要: 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.222All datasets, code, and the Extended version for scCluBench are available at the link: https://github.com/XPgogogo/scCluBench. More details for each stage are provided in the extended version.