arXiv:2602.04270cs.LGq-bio.NC2026-02被引 1

跨类别标签融合分析时间序列,分离不同标签对数据的影响。

Multi-Integration of Labels across Categories for Component Identification (MILCCI)

  • 基于标签相似性构建稀疏分解,动态调整成分构成。
  • 可捕捉跨试验的变异性,学习随时间演变的成分轨迹。
  • 适用于神经记录、投票行为等多类别标签场景。

许多领域通过重复测量(试验)收集大规模时间序列数据,每项试验关联多个类别标签(如任务难度、动物选择)。核心挑战在于理解这些标签如何编码于多试验观测中,并分离各标签类别对数据的独立影响。本文提出MILCCI,一种数据驱动方法:(i)识别数据背后的可解释成分,(ii)捕捉跨试验变异,(iii)融合标签信息解析各类别在数据中的表征。MILCCI扩展了稀疏逐试验分解,利用每类内部标签相似性,实现细微、标签引导的成分组合调整,以区分各类别贡献。同时,它学习每个成分随时间演化且跨试验灵活变化的时序轨迹。我们在合成数据及真实案例(包括投票模式、网页访问趋势、神经元记录)中验证其性能。

原文摘要 · Abstract (English)

Many fields collect large-scale temporal data through repeated measurements (trials), where each trial is labeled with a set of metadata variables spanning several categories. For example, a trial in a neuroscience study may be linked to a value from category (a): task difficulty, and category (b): animal choice. A critical challenge in time-series analysis is to understand how these labels are encoded within the multi-trial observations, and disentangle the distinct effect of each label entry across categories. Here, we present MILCCI, a novel data-driven method that i) identifies the interpretable components underlying the data, ii) captures cross-trial variability, and iii) integrates label information to understand each category's representation within the data. MILCCI extends a sparse per-trial decomposition that leverages label similarities within each category to enable subtle, label-driven cross-trial adjustments in component compositions and to distinguish the contribution of each category. MILCCI also learns each component's corresponding temporal trace, which evolves over time within each trial and varies flexibly across trials. We demonstrate MILCCI's performance through both synthetic and real-world examples, including voting patterns, online page view trends, and neuronal recordings.

时间序列成分分析标签融合神经科学

Thank you to arXiv for use of its open access interoperability. PaperDance 不是 arXiv 官方产品;中文卡片由大模型生成,请以原文为准。