Evidence map›Paper›PMID 40778314›Full record

ArticleComputational and structural biotechnology journal2025

PCLDA: An interpretable cell annotation tool for single-cell RNA-sequencing data based on simple statistical methods.

Kailun Bai, Belaid Moa, Xiaojian Shao, Xuekui Zhang

Abstract read
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Article in Computational and structural biotechnology journal, 2025. 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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0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kailun BaiDepartment of Mathematics and Statistics, University of Victoria, Victoria BC, Canada.
Belaid MoaDigital Research Alliance of Canada, Victoria BC, Canada.
Xiaojian ShaoDepartment of Mathematics and Statistics, University of Victoria, Victoria BC, Canada.
Xuekui ZhangDepartment of Mathematics and Statistics, University of Victoria, Victoria BC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) enables high-resolution analysis of cellular heterogeneity, yet accurate and consistent cell-type annotation remains a crucial challenge. Numerous automated tools exist, but their complex modeling assumptions can hinder reliability across varied datasets and protocols. We propose PCLDA, a pipeline composed of three modules: t-test-based gene screening, principal component analysis (PCA) and linear discriminant analysis (LDA), all built on simple statistical methods. An ablation study shows that each module in PCLDA contributes significantly to performance and robustness, with two novel enhancements in the second module yielding substantial gains. Despite these additions, the model retains its original assumptions, computational efficiency, and interpretability. Benchmarking against nine state-of-the-art methods across 22 public scRNA-seq datasets and 35 distinct evaluation scenarios, PCLDA consistently achieves top-tier accuracy under both intra-dataset (cross-validation) and inter-dataset (cross-platform) conditions. Notably, when reference and query data are generated via different protocols, PCLDA remains stable and often outperforms more complex machine-learning approaches. Furthermore, PCLDA offers strong interpretability, attributed to the linear nature of its PCA and LDA modules. The final decision boundaries are linear combinations of the original gene expression values, directly reflecting the contribution of each gene to the classification. Top-weighted genes identified by PCLDA better capture biologically meaningful signals in enrichment analyses than those selected via marginal screening alone, offering deeper functional insights into cell-type specificity. In conclusion, our work underscores the utility of carefully enhanced simple statistics methods for single-cell annotation. PCLDA's simplicity, interpretability, and consistently high performance make it a practical, reliable alternative to more complex annotation pipelines. Code is available on GitHub:https://github.com/kellen8hao/PCLDA.

Indexed as

Cell type annotationInterpretable machine learningLinear discriminant analysisSimple statisticsSingle-cell genomics

Identifiers

PMID40778314
PMCPMC12329077

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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.