Evidence map›Paper›PMID 38924517›Full record

ArticleBioinformatics (Oxford, England)2024

PredGCN: a Pruning-enabled Gene-Cell Net for automatic cell annotation of single cell transcriptome data.

Qi Qi, Yunhe Wang, Yujian Huang, Yi Fan, Xiangtao Li

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Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Qi QiSchool of Artificial Intelligence, Jilin University, Changchun 130012, China.
Yunhe WangSchool of Artificial Intelligence, Hebei University of Technology, Tianjin 300401, China.
Yujian HuangCollege of Computer Science and Cyber Security, Chengdu University of Technology, Chengdu 610059, China.
Yi FanSchool of Artificial Intelligence, Jilin University, Changchun 130012, China.ORCID 0000-0001-8620-2735
Xiangtao LiSchool of Artificial Intelligence, Jilin University, Changchun 130012, China.ORCID 0000-0002-8716-9823

Funding

Jilin Province Outstanding Young Scientist Program 20230508098RCNational Natural Science Foundation of China 62076109
6 · The paper itself

Abstract

motivationThe annotation of cell types from single-cell transcriptomics is essential for understanding the biological identity and functionality of cellular populations. Although manual annotation remains the gold standard, the advent of automatic pipelines has become crucial for scalable, unbiased, and cost-effective annotations. Nonetheless, the effectiveness of these automatic methods, particularly those employing deep learning, significantly depends on the architecture of the classifier and the quality and diversity of the training datasets.

resultsTo address these limitations, we present a Pruning-enabled Gene-Cell Net (PredGCN) incorporating a Coupled Gene-Cell Net (CGCN) to enable representation learning and information storage. PredGCN integrates a Gene Splicing Net (GSN) and a Cell Stratification Net (CSN), employing a pruning operation (PrO) to dynamically tackle the complexity of heterogeneous cell identification. Among them, GSN leverages multiple statistical and hypothesis-driven feature extraction methods to selectively assemble genes with specificity for scRNA-seq data while CSN unifies elements based on diverse region demarcation principles, exploiting the representations from GSN and precise identification from different regional homogeneity perspectives. Furthermore, we develop a multi-objective Pareto pruning operation (Pareto PrO) to expand the dynamic capabilities of CGCN, optimizing the sub-network structure for accurate cell type annotation. Multiple comparison experiments on real scRNA-seq datasets from various species have demonstrated that PredGCN surpasses existing state-of-the-art methods, including its scalability to cross-species datasets. Moreover, PredGCN can uncover unknown cell types and provide functional genomic analysis by quantifying the influence of genes on cell clusters, bringing new insights into cell type identification and characterizing scRNA-seq data from different perspectives. AVAILABILITY AND IMPLEMENTATION: The source code is available at https://github.com/IrisQi7/PredGCN and test data is available at https://figshare.com/articles/dataset/PredGCN/25251163.

Indexed as

Single-Cell AnalysisTranscriptomeAlgorithmsAnimalsComputational BiologyGene Expression ProfilingHumansMolecular Sequence AnnotationSoftware

Identifiers

PMID38924517
PMCPMC11236098

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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.