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arXiv 2311.02455cs.LGq-bio.GNq-bio.QMstat.AP
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融合多示例学习的混合模型

Mixed Models with Multiple Instance Learning

Helmholtz Munich(亥姆霍兹慕尼黑);Eindhoven University of Technology(埃因霍温理工大学)

Jan P. Engelmann, Alessandro Palma, Jakub M. Tomczak, Fabian J. Theis, Francesco Paolo Casale

AI总结:

针对现有单细胞患者特征预测方法忽略细胞异质性的问题,提出整合GLMM和MIL的MixMIL框架,利用预定义细胞嵌入兼顾效率与异质性建模,在单细胞数据集上性能优于现有MIL模型,可发现新关联并阐明生物学机制。

摘要:

从单细胞数据预测患者特征有助于识别与健康和疾病相关的细胞状态。该任务通常采用线性模型和平均细胞类型表达,因其高效且稳健,但它们忽略了单细胞数据固有的丰富细胞异质性。为弥补这一不足,我们提出MixMIL,这是一个整合广义线性混合模型(GLMM)和多示例学习(MIL)的框架,在保留线性模型优势的同时对细胞状态异质性建模。通过利用预定义的细胞嵌入,MixMIL提升了计算效率,并与单细胞表示学习的最新进展相契合。我们的实验结果表明,MixMIL在单细胞数据集上优于现有MIL模型,能够发现新的关联并阐明不同领域的生物学机制。

英文摘要:

Predicting patient features from single-cell data can help identify cellular states implicated in health and disease. Linear models and average cell type expressions are typically favored for this task for their efficiency and robustness, but they overlook the rich cell heterogeneity inherent in single-cell data. To address this gap, we introduce MixMIL, a framework integrating Generalized Linear Mixed Models (GLMM) and Multiple Instance Learning (MIL), upholding the advantages of linear models while modeling cell state heterogeneity. By leveraging predefined cell embeddings, MixMIL enhances computational efficiency and aligns with recent advancements in single-cell representation learning. Our empirical results reveal that MixMIL outperforms existing MIL models in single-cell datasets, uncovering new associations and elucidating biological mechanisms across different domains.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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