GenoCraft: A Comprehensive, User-Friendly Web-Based Platform for High-Throughput Omics Data Analysis and VisualizationYingzhou Lu, Minjie Shen, Ling Yue et al.
The surge in high-throughput omics data has reshaped the landscape of biological research, underlining the need for powerful, user-friendly data analysis and interpretation tools. This paper presents GenoCraft, a web-based comprehensive software solution designed to handle the entire pipeline of omics data processing. GenoCraft offers a unified platform featuring advanced bioinformatics tools, covering all aspects of omics data analysis. It encompasses a range of functionalities, such as normalization, quality control, differential analysis, network analysis, pathway analysis, and diverse visualization techniques. This software makes state-of-the-art omics data analysis more accessible to a wider range of users. With GenoCraft, researchers and data scientists have access to an array of cutting-edge bioinformatics tools under a user-friendly interface, making it a valuable resource for managing and analyzing large-scale omics data. The API with an interactive web interface is publicly available at https://genocraft.stanford. edu/. We also release all the codes in https://github.com/futianfan/GenoCraft.
2.7CLJul 11, 2025
Knowledge Fusion via Bidirectional Information AggregationSonglin Zhai, Guilin Qi, Yue Wang et al.
Knowledge graphs (KGs) are the cornerstone of the semantic web, offering up-to-date representations of real-world entities and relations. Yet large language models (LLMs) remain largely static after pre-training, causing their internal knowledge to become outdated and limiting their utility in time-sensitive web applications. To bridge this gap between dynamic knowledge and static models, a prevalent approach is to enhance LLMs with KGs. However, prevailing methods typically rely on parameter-invasive fine-tuning, which risks catastrophic forgetting and often degrades LLMs' general capabilities. Moreover, their static integration frameworks cannot keep pace with the continuous evolution of real-world KGs, hindering their deployment in dynamic web environments. To bridge this gap, we introduce KGA (\textit{\underline{K}nowledge \underline{G}raph-guided \underline{A}ttention}), a novel framework that dynamically integrates external KGs into LLMs exclusively at inference-time without any parameter modification. Inspired by research on neuroscience, we rewire the self-attention module by innovatively introducing two synergistic pathways: a \textit{bottom-up knowledge fusion} pathway and a \textit{top-down attention guidance} pathway. The \textit{bottom-up pathway} dynamically integrates external knowledge into input representations via input-driven KG fusion, which is akin to the \textit{stimulus-driven attention process} in the human brain. Complementarily, the \textit{top-down pathway} aims to assess the contextual relevance of each triple through a \textit{goal-directed verification process}, thereby suppressing task-irrelevant signals and amplifying knowledge-relevant patterns. By synergistically combining these two pathways, our method supports real-time knowledge fusion. Extensive experiments on four benchmarks verify KGA's strong fusion performance and efficiency.
10.3MLAug 9, 2017
Maximum Volume Inscribed Ellipsoid: A New Simplex-Structured Matrix Factorization Framework via Facet Enumeration and Convex OptimizationChia-Hsiang Lin, Ruiyuan Wu, Wing-Kin Ma et al.
Consider a structured matrix factorization model where one factor is restricted to have its columns lying in the unit simplex. This simplex-structured matrix factorization (SSMF) model and the associated factorization techniques have spurred much interest in research topics over different areas, such as hyperspectral unmixing in remote sensing, topic discovery in machine learning, to name a few. In this paper we develop a new theoretical SSMF framework whose idea is to study a maximum volume ellipsoid inscribed in the convex hull of the data points. This maximum volume inscribed ellipsoid (MVIE) idea has not been attempted in prior literature, and we show a sufficient condition under which the MVIE framework guarantees exact recovery of the factors. The sufficient recovery condition we show for MVIE is much more relaxed than that of separable non-negative matrix factorization (or pure-pixel search); coincidentally it is also identical to that of minimum volume enclosing simplex, which is known to be a powerful SSMF framework for non-separable problem instances. We also show that MVIE can be practically implemented by performing facet enumeration and then by solving a convex optimization problem. The potential of the MVIE framework is illustrated by numerical results.
1.4MLJun 28, 2014
Convex Analysis of Mixtures for Separating Non-negative Well-grounded SourcesYitan Zhu, Niya Wang, David J. Miller et al.
Blind Source Separation (BSS) has proven to be a powerful tool for the analysis of composite patterns in engineering and science. We introduce Convex Analysis of Mixtures (CAM) for separating non-negative well-grounded sources, which learns the mixing matrix by identifying the lateral edges of the convex data scatter plot. We prove a sufficient and necessary condition for identifying the mixing matrix through edge detection, which also serves as the foundation for CAM to be applied not only to the exact-determined and over-determined cases, but also to the under-determined case. We show the optimality of the edge detection strategy, even for cases where source well-groundedness is not strictly satisfied. The CAM algorithm integrates plug-in noise filtering using sector-based clustering, an efficient geometric convex analysis scheme, and stability-based model order selection. We demonstrate the principle of CAM on simulated data and numerically mixed natural images. The superior performance of CAM against a panel of benchmark BSS techniques is demonstrated on numerically mixed gene expression data. We then apply CAM to dissect dynamic contrast-enhanced magnetic resonance imaging data taken from breast tumors and time-course microarray gene expression data derived from in-vivo muscle regeneration in mice, both producing biologically plausible decomposition results.