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Abstract
Motivation: Single-cell RNA sequencing (scRNA-seq) methods make it possible to reveal gene expression patterns at single-cell resolution. Due to technical defects, dropout events in scRNA-seq will add noise to the gene-cell expression matrix and hinder downstream analysis. Therefore, it is important for recovering the true gene expression levels before carrying out downstream analysis.
Results: In this article, we develop an imputation method, called scTSSR, to recover gene expression for scRNA-seq. Unlike most existing methods that impute dropout events by borrowing information across only genes or cells, scTSSR simultaneously leverages information from both similar genes and similar cells using a two-side sparse self-representation model. We demonstrate that scTSSR can effectively capture the Gini coefficients of genes and gene-to-gene correlations observed in single-molecule RNA fluorescence in situ hybridization (smRNA FISH). Down-sampling experiments indicate that scTSSR performs better than existing methods in recovering the true gene expression levels. We also show that scTSSR has a competitive performance in differential expression analysis, cell clustering and cell trajectory inference.
Availability and implementation: The R package is available at https://github.com/Zhangxf-ccnu/scTSSR.
Contact: [email protected]
Supplementary information: Supplementary data are available at Bioinformatics online.
Results: In this article, we develop an imputation method, called scTSSR, to recover gene expression for scRNA-seq. Unlike most existing methods that impute dropout events by borrowing information across only genes or cells, scTSSR simultaneously leverages information from both similar genes and similar cells using a two-side sparse self-representation model. We demonstrate that scTSSR can effectively capture the Gini coefficients of genes and gene-to-gene correlations observed in single-molecule RNA fluorescence in situ hybridization (smRNA FISH). Down-sampling experiments indicate that scTSSR performs better than existing methods in recovering the true gene expression levels. We also show that scTSSR has a competitive performance in differential expression analysis, cell clustering and cell trajectory inference.
Availability and implementation: The R package is available at https://github.com/Zhangxf-ccnu/scTSSR.
Contact: [email protected]
Supplementary information: Supplementary data are available at Bioinformatics online.
| Original language | English |
|---|---|
| Pages (from-to) | 3131-3138 |
| Journal | Bioinformatics |
| Volume | 36 |
| Issue number | 10 |
| Online published | 19 Feb 2020 |
| DOIs | |
| Publication status | Published - 15 May 2020 |
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- 2 Finished
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GRF: Investigation of EGFR Inter-domain Relations and Their Roles in Lung Cancer Drug Resistance
YAN, H. (Principal Investigator / Project Coordinator)
1/01/19 → 9/06/23
Project: Research
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CRF: Efficient Algorithms and Hardware Accelerators for Tensor Decomposition and Their Applications to Multidimensional Data Analysis
YAN, H. (Principal Investigator / Project Coordinator), CHEUNG, C. C. R. (Co-Principal Investigator), CHAN, R. H. F. (Co-Investigator), LEE, V. H. F. (Co-Investigator), NG, M. K. P. (Co-Investigator) & QI, L. (Co-Investigator)
1/06/16 → 9/11/20
Project: Research