Hierarchical marker genes selection in scRNA-seq analysis

When analyzing scRNA-seq data containing heterogeneous cell populations, an important task is to select informative marker genes to distinguish various cell clusters and annotate the clusters with biologically meaningful cell types. In existing analysis methods and pipelines, marker genes are typically identified using a one-vs-all strategy, examining differential expression between one cell cluster versus the combination of all other cell clusters. However, this strategy applied to cell clusters belonging to closely related cell types often generates overlapping marker genes, which capture the common signature of closely related cell clusters but provide limited information for distinguishing them. To address the limitations of the one-vs-all strategy, we propose a hierarchical marker gene selection strategy that groups similar cell clusters and selects marker genes in a hierarchical manner. This strategy is able to improve the accuracy and interpretability of cell type identification in single-cell RNA-seq data.

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Publication Details

Journal
PLoS Computational Biology
Published
2024-12-12
DOI
https://doi.org/10.1371/journal.pcbi.1012643
Citations
2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.47

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article

Hierarchical marker genes selection in scRNA-seq analysis

Peng Qiu, Yutong Sun
2 citations
PLoS Computational Biology
Single-cell and spatial transcriptomics
0.47
article

Hierarchical marker genes selection in scRNA-seq analysis

Peng Qiu, Yutong Sun
article en
2 citations

Abstract

When analyzing scRNA-seq data containing heterogeneous cell populations, an important task is to select informative marker genes to distinguish various cell clusters and annotate the clusters with biologically meaningful cell types. In existing analysis methods and pipelines, marker genes are typically identified using a one-vs-all strategy, examining differential expression between one cell cluster versus the combination of all other cell clusters. However, this strategy applied to cell clusters belonging to closely related cell types often generates overlapping marker genes, which capture the common signature of closely related cell clusters but provide limited information for distinguishing them. To address the limitations of the one-vs-all strategy, we propose a hierarchical marker gene selection strategy that groups similar cell clusters and selects marker genes in a hierarchical manner. This strategy is able to improve the accuracy and interpretability of cell type identification in single-cell RNA-seq data.

PLoS Computational BiologyVol. 20(12)
Georgia Institute of Technology (US), Emory University (US)
National Science Foundation, Georgia Institute of Technology, Leona M. and Harry B. Helmsley Charitable Trust, Division of Computing and Communication Foundations
Openalex Percentile: Top 34%
Single-cell and spatial transcriptomics
0.47
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