Evidence map›Paper›PMID 36564711›Full record

ArticleBMC genomics2022

Non-negative low-rank representation based on dictionary learning for single-cell RNA-sequencing data analysis.

Juan Wang, Nana Zhang, Shasha Yuan, Junliang Shang, Lingyun Dai, Feng Li, Jinxing Liu

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In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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3 · Its place in the literature

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4 citing papers in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Juan WangSchool of Computer Science, Qufu Normal University, Rizhao, China.
Nana ZhangSchool of Computer Science, Qufu Normal University, Rizhao, China.
Shasha YuanSchool of Computer Science, Qufu Normal University, Rizhao, China.
Junliang ShangSchool of Computer Science, Qufu Normal University, Rizhao, China.
Lingyun DaiSchool of Computer Science, Qufu Normal University, Rizhao, China.
Feng LiSchool of Computer Science, Qufu Normal University, Rizhao, China.
Jinxing LiuSchool of Computer Science, Qufu Normal University, Rizhao, China. sdcavell@126.com.

Funding

National Natural Science Foundation of China 61902215National Natural Science Foundation of China 61902216National Natural Science Foundation of China 61972226National Natural Science Foundation of China 62172253National Natural Science Foundation of China 62172254
6 · The paper itself

Abstract

In the analysis of single-cell RNA-sequencing (scRNA-seq) data, how to effectively and accurately identify cell clusters from a large number of cell mixtures is still a challenge. Low-rank representation (LRR) method has achieved excellent results in subspace clustering. But in previous studies, most LRR-based methods usually choose the original data matrix as the dictionary. In addition, the methods based on LRR usually use spectral clustering algorithm to complete cell clustering. Therefore, there is a matching problem between the spectral clustering method and the affinity matrix, which is difficult to ensure the optimal effect of clustering. Considering the above two points, we propose the DLNLRR method to better identify the cell type. First, DLNLRR can update the dictionary during the optimization process instead of using the predefined fixed dictionary, so it can realize dictionary learning and LRR learning at the same time. Second, DLNLRR can realize subspace clustering without relying on spectral clustering algorithm, that is, we can perform clustering directly based on the low-rank matrix. Finally, we carry out a large number of experiments on real single-cell datasets and experimental results show that DLNLRR is superior to other scRNA-seq data analysis algorithms in cell type identification.

Indexed as

AlgorithmsLearningCluster AnalysisData AnalysisRNASequence Analysis, RNASingle-Cell AnalysisRNACell type identificationDictionary learningLow-rank representationscRNA-seq data analysisSubspace clustering

Identifiers

PMID36564711
PMCPMC9789616

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