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Sparsity-Penalized Stacked Denoising Autoencoders for Imputing Single-Cell RNA-seq Data

机译:用于插补单细胞RNA-seq数据的稀疏惩罚堆叠式去噪自动编码器

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摘要

Single-cell RNA-seq (scRNA-seq) is quite prevalent in studying transcriptomes, but it suffers from excessive zeros, some of which are true, but others are false. False zeros, which can be seen as missing data, obstruct the downstream analysis of single-cell RNA-seq data. How to distinguish true zeros from false ones is the key point of this problem. Here, we propose sparsity-penalized stacked denoising autoencoders (scSDAEs) to impute scRNA-seq data. scSDAEs adopt stacked denoising autoencoders with a sparsity penalty, as well as a layer-wise pretraining procedure to improve model fitting. scSDAEs can capture nonlinear relationships among the data and incorporate information about the observed zeros. We tested the imputation efficiency of scSDAEs on recovering the true values of gene expression and helping downstream analysis. First, we show that scSDAE can recover the true values and the sample–sample correlations of bulk sequencing data with simulated noise. Next, we demonstrate that scSDAEs accurately impute RNA mixture dataset with different dilutions, spike-in RNA concentrations affected by technical zeros, and improves the consistency of RNA and protein levels in CITE-seq data. Finally, we show that scSDAEs can help downstream clustering analysis. In this study, we develop a deep learning-based method, scSDAE, to impute single-cell RNA-seq affected by technical zeros. Furthermore, we show that scSDAEs can recover the true values, to some extent, and help downstream analysis.
机译:单细胞RNA-seq(scRNA-seq)在研究转录组中非常普遍,但是它遭受了过多的零,其中一些是正确的,而其他则是错误的。错误的零(可以看作是丢失的数据)阻碍了单细胞RNA-seq数据的下游分析。如何区分真零和假零是这个问题的关键。在这里,我们提出了稀疏惩罚堆叠式去噪自动编码器(scSDAEs)来插补scRNA-seq数据。 scSDAE采用具有稀疏惩罚的堆叠式去噪自动编码器,以及分层的预训练程序以改善模型拟合。 scSDAE可以捕获数据之间的非线性关系,并合并有关观测到的零的信息。我们测试了scSDAEs在恢复基因表达真实值和帮助下游分析方面的估算效率。首先,我们证明scSDAE可以恢复真实值以及具有模拟噪声的大量测序数据的样品-样品相关性。接下来,我们证明scSDAEs可以准确估算具有不同稀释度的RNA混合物数据集,掺入的RNA浓度受技术零值的影响,并提高了CITE-seq数据中RNA和蛋白质水平的一致性。最后,我们证明了scSDAE可以帮助进行下游聚类分析。在这项研究中,我们开发了一种基于深度学习的方法scSDAE,用于估算受技术零影响的单细胞RNA-seq。此外,我们表明scSDAEs可以在一定程度上恢复真实值,并有助于下游分析。

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