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Ensemble dimensionality reduction and feature gene extraction for single-cell RNA-seq data

机译:单细胞RNA-SEQ数据的合并维数减少和特征基因提取

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Single-cell RNA sequencing (scRNA-seq) technologies allow researchers to uncover the biological states of a single cell at high resolution. For computational efficiency and easy visualization, dimensionality reduction is necessary to capture gene expression patterns in low-dimensional space. Here we propose an ensemble method for simultaneous dimensionality reduction and feature gene extraction (EDGE) of scRNA-seq data. Different from existing dimensionality reduction techniques, the proposed method implements an ensemble learning scheme that utilizes massive weak learners for an accurate similarity search. Based on the similarity matrix constructed by those weak learners, the low-dimensional embedding of the data is estimated and optimized through spectral embedding and stochastic gradient descent. Comprehensive simulation and empirical studies show that EDGE is well suited for searching for meaningful organization of cells, detecting rare cell types, and identifying essential feature genes associated with certain cell types. Dimensionality reduction is used to make the analysis of single-cell RNA sequencing data more efficient. Here the authors propose a method, EDGE, which simultaneously carries out dimensionality reduction and feature gene extraction.
机译:单细胞RNA测序(SCRNA-SEQ)技术允许研究人员在高分辨率下揭示单个细胞的生物状态。为了计算效率和易于可视化,捕获低维空间中的基因表达模式是必要的维度降低。在这里,我们提出了一种用于同时减少的组合方法,具有SCRNA-SEQ数据的同时降低和特征基因提取(边缘)。不同于现有的维度减少技术,所提出的方法实现了一种合并学习方案,该方案利用大规模弱学习者进行准确的相似性搜索。基于这些弱学习者构建的相似性矩阵,通过光谱嵌入和随机梯度下降来估计和优化数据的低维嵌入。综合模拟和实证研究表明,边缘非常适合于寻找有意义的细胞组织,检测稀有细胞类型,并识别与某些细胞类型相关的基本特征基因。维度减少用于更有效地分析单细胞RNA测序数据。这里作者提出了一种方法,边缘,其同时进行维度降低和特征基因提取。

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