Evidence map›Paper›PMID 39680741›Full record

ArticleBriefings in bioinformatics2024

GSTRPCA: irregular tensor singular value decomposition for single-cell multi-omics data clustering.

Lubin Cui, Guiliang Guo, Michael K Ng, Quan Zou, Yushan Qiu

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Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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8citing papers in PubMed
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8 citing papers in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Lubin CuiSchool of Mathematics and Statistics, Henan Normal University, Xinxiang 453007, China.
Guiliang GuoSchool of Mathematics and Statistics, Henan Normal University, Xinxiang 453007, China.
Michael K NgDepartment of Mathematics, Hong Kong Baptist University, Hong Kong 999077, China.
Quan ZouInstitute of Fundamental and Frontier Sciences, Electronic Science and Technology University, Chengdu 611731, China.
Yushan QiuSchool of Mathematical Sciences, Shenzhen University, Guangdong 518000, China.

Funding

Guangdong Basic and Applied Basic Research Foundation 2024A1515010113National Natural Science Foundation of China 62372303National Natural Science Foundation of Henan Province 242300420251Shenzhen Science and Technology Program RCYX20231211090244048
6 · The paper itself

Abstract

Single-cell multi-omics refers to the various types of biological data at the single-cell level. These data have enabled insight and resolution to cellular phenotypes, biological processes, and developmental stages. Current advances hold high potential for breakthroughs by integrating multiple different omics layers. However, singlecell multi-omics data usually have different feature dimensions and direct or indirect relationships. How to keep the data structure of these different data and extract hidden relationships is a major challenge for omics data integration, and effective integration models are urgently needed. In this paper, we propose an irregular tensor decomposition model (GSTRPCA) based on tensor robust principal component analysis (TRPCA). We developed a weighted threshold model for the decomposition of irregular tensor data by combining low-rank and sparsity constraints, which requires that the low-dimensional embeddings of the data remain lowrank and sparse. The major advantage of the GSTRPCA algorithm is its ability to keep the original data structure and explore hidden related features among omics data. For GSTRPCA, we also designed an effective algorithm that theoretically guarantees global convergence for the tensor decomposition. The computational experiments on irregular tensor datasets demonstrate that GSTRPCA significantly outperformed the state-of-the-art methods and hence confirm the superiority of GSTRPCA in clustering single-cell multiomics data. To our knowledge, this is the first tensor decomposition method for irregular tensor data to keep the data structure and hence improve the clustering performance for single-cell multi-omics data. GSTRPCA is a Matlabbased algorithm, and the code is available from https://github.com/GGL-B/GSTRPCA.

Indexed as

AlgorithmsPrincipal Component AnalysisSingle-Cell AnalysisCluster AnalysisComputational BiologyGenomicsHumansMultiomicsirregular tensor decompositionjoint tensorsingle-cell multi-omics dataweighted threshold

Identifiers

PMID39680741
PMCPMC11647523

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.