{"title":"DEAPLOG: Differential Expression Analysis and Pseudo-Temporal Locating and Ordering of Genes in Single-Cell Transcriptomic Data.","authors":"Bao Zhang, Jing Wang, Weiwei Wang, Hongbo Zhang","doi":"10.1007/s12539-025-00778-4","DOIUrl":null,"url":null,"abstract":"<p><p>Differential expression analysis constitutes a crucial step in the analysis of single-cell transcriptomic data. Numerous statistical methods have been developed to conduct differential expression analysis by addressing the sparsity or heterogeneity of gene expression. Nevertheless, these approaches often overlook other critical characteristics of single-cell transcriptomic data, such as the high dimensionality of gene expression at the cellular level, which may consequently lead to suboptimal performance. Furthermore, to date, there remains a significant gap in methodologies capable of locating and ordering genes along cell trajectories. Here, we integrate polynomial fitting with hypergeometric testing to develop a new tool, DEAPLOG (Differential Expression Analysis and Pseudo-temporal Locating and Ordering of Genes), leveraging the high-dimensional gene expression characteristics at the cellular level in single-cell transcriptomic data. Benchmarking analyses on synthetic single-cell datasets demonstrate that while DEAPLOG exhibits performance comparable to existing methods on datasets comprising only two cell clusters, it demonstrates superior performance in differential expression analysis when applied to datasets with multiple cell clusters. Furthermore, the applications of DEAPLOG to real single-cell and spatial transcriptomic dataset not only validate its superior performance in terms of accuracy but also computational efficiency. Notably, when applied to single-cell transcriptomic data from the developmental hematopoietic system, DEAPLOG demonstrate precise gene localization and accurate ordering along developmental trajectories. Collectively, these findings establish DEAPLOG as a robust and highly effective tool for single-cell transcriptomic data analysis.</p>","PeriodicalId":13670,"journal":{"name":"Interdisciplinary Sciences: Computational Life Sciences","volume":" ","pages":"822-837"},"PeriodicalIF":5.2000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Interdisciplinary Sciences: Computational Life Sciences","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s12539-025-00778-4","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Differential expression analysis constitutes a crucial step in the analysis of single-cell transcriptomic data. Numerous statistical methods have been developed to conduct differential expression analysis by addressing the sparsity or heterogeneity of gene expression. Nevertheless, these approaches often overlook other critical characteristics of single-cell transcriptomic data, such as the high dimensionality of gene expression at the cellular level, which may consequently lead to suboptimal performance. Furthermore, to date, there remains a significant gap in methodologies capable of locating and ordering genes along cell trajectories. Here, we integrate polynomial fitting with hypergeometric testing to develop a new tool, DEAPLOG (Differential Expression Analysis and Pseudo-temporal Locating and Ordering of Genes), leveraging the high-dimensional gene expression characteristics at the cellular level in single-cell transcriptomic data. Benchmarking analyses on synthetic single-cell datasets demonstrate that while DEAPLOG exhibits performance comparable to existing methods on datasets comprising only two cell clusters, it demonstrates superior performance in differential expression analysis when applied to datasets with multiple cell clusters. Furthermore, the applications of DEAPLOG to real single-cell and spatial transcriptomic dataset not only validate its superior performance in terms of accuracy but also computational efficiency. Notably, when applied to single-cell transcriptomic data from the developmental hematopoietic system, DEAPLOG demonstrate precise gene localization and accurate ordering along developmental trajectories. Collectively, these findings establish DEAPLOG as a robust and highly effective tool for single-cell transcriptomic data analysis.
期刊介绍:
Interdisciplinary Sciences--Computational Life Sciences aims to cover the most recent and outstanding developments in interdisciplinary areas of sciences, especially focusing on computational life sciences, an area that is enjoying rapid development at the forefront of scientific research and technology.
The journal publishes original papers of significant general interest covering recent research and developments. Articles will be published rapidly by taking full advantage of internet technology for online submission and peer-reviewing of manuscripts, and then by publishing OnlineFirstTM through SpringerLink even before the issue is built or sent to the printer.
The editorial board consists of many leading scientists with international reputation, among others, Luc Montagnier (UNESCO, France), Dennis Salahub (University of Calgary, Canada), Weitao Yang (Duke University, USA). Prof. Dongqing Wei at the Shanghai Jiatong University is appointed as the editor-in-chief; he made important contributions in bioinformatics and computational physics and is best known for his ground-breaking works on the theory of ferroelectric liquids. With the help from a team of associate editors and the editorial board, an international journal with sound reputation shall be created.