scIDS: Single-cell Imputation by combining Deep autoencoder neural networks and Subspace regression

Bang Tran, Quyen Nguyen, Sangam Shrestha, Tin Nguyen
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引用次数: 0

Abstract

Single-cell RNA-sequencing (scRNA-seq) has emerged as a powerful high throughput technique that enables the characterization of transcriptomic profiles at single-cell resolution. However, scRNA-seq data has an excess number of zeros in expressed genes due to a low amount of sequenced mRNA in each cell. This missing detection in a portion of mRNA molecules (dropout) presents a fundamental challenge for various types of data analyses. Here we introduce scIDS, a novel imputation method that is a combination of deep autoencoder neural networks and subspace regression to reliably recover the missing values in scRNA-seq data. We compare scIDS with two widely used methods using eight datasets. Extensive experiments demonstrate that scIDS outperforms existing approaches in improving the identification of cell populations while preserving the biological landscape.
scIDS:结合深度自编码器神经网络和子空间回归的单细胞输入
单细胞rna测序(scRNA-seq)已经成为一种强大的高通量技术,可以在单细胞分辨率下表征转录组谱。然而,由于每个细胞中测序mRNA的数量较少,scRNA-seq数据中表达基因的零数量过多。这种缺失检测mRNA分子的一部分(dropout)提出了各种类型的数据分析的基本挑战。本文介绍了一种将深度自编码器神经网络与子空间回归相结合的scIDS方法,该方法可以可靠地恢复scRNA-seq数据中的缺失值。我们使用8个数据集将scIDS与两种广泛使用的方法进行比较。广泛的实验表明,scIDS在改善细胞群识别同时保护生物景观方面优于现有方法。
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