{"title":"基于细胞间相互作用的轨迹推断(TICCI):细胞间通信提高了轨迹推断方法的准确性。","authors":"Yifeng Fu, Hong Qu, Dacheng Qu, Min Zhao","doi":"10.1093/bioinformatics/btaf027","DOIUrl":null,"url":null,"abstract":"<p><strong>Motivation: </strong>Understanding cell differentiation and development dynamics is key for single-cell transcriptome analysis. Current cell differentiation trajectory inference algorithms face challenges such as high dimensionality, noise, and a need for users to possess certain biological information about the datasets to effectively utilize the algorithms. Here, we introduce Trajectory Inference with Cell-Cell Interaction (TICCI), a novel way to address these challenges by integrating intercellular communication information. In recognizing crucial intercellular communication during development, TICCI proposes Cell-Cell Interactions (CCI) at single-cell resolution. We posit that cells exhibiting higher gene expression similarity patterns are more likely to exchange information via biomolecular mediators.</p><p><strong>Results: </strong>TICCI is initiated by constructing a cell-neighborhood matrix using edge weights composed of intercellular similarity and CCI information. Louvain partitioning identifies trajectory branches, attenuating noise, while single-cell entropy (scEntropy) is used to assess differentiation status. The Chu-Liu algorithm constructs a directed least-square model to identify trajectory branches, and an improved diffusion fitted time algorithm computes cell-fitted time in nonconnected topologies. TICCI validation on single-cell RNA sequencing (scRNA-seq) datasets confirms the accuracy of cell trajectories, aligning with genealogical branching and gene markers. Verification using extrinsic information labels demonstrates CCI information utility in enhancing accurate trajectory inference. A comparative analysis establishes TICCI proficiency in accurate temporal ordering.</p><p><strong>Availability and implementation: </strong>Source code and binaries freely available for download at https://github.com/mine41/TICCI, implemented in R (version 4.32) and Python (version 3.7.16) and supported on MS Windows. Authors ensure that the software is available for a full two years following publication.</p>","PeriodicalId":93899,"journal":{"name":"Bioinformatics (Oxford, England)","volume":" ","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2025-02-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11829803/pdf/","citationCount":"0","resultStr":"{\"title\":\"Trajectory Inference with Cell-Cell Interactions (TICCI): intercellular communication improves the accuracy of trajectory inference methods.\",\"authors\":\"Yifeng Fu, Hong Qu, Dacheng Qu, Min Zhao\",\"doi\":\"10.1093/bioinformatics/btaf027\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Motivation: </strong>Understanding cell differentiation and development dynamics is key for single-cell transcriptome analysis. Current cell differentiation trajectory inference algorithms face challenges such as high dimensionality, noise, and a need for users to possess certain biological information about the datasets to effectively utilize the algorithms. Here, we introduce Trajectory Inference with Cell-Cell Interaction (TICCI), a novel way to address these challenges by integrating intercellular communication information. In recognizing crucial intercellular communication during development, TICCI proposes Cell-Cell Interactions (CCI) at single-cell resolution. We posit that cells exhibiting higher gene expression similarity patterns are more likely to exchange information via biomolecular mediators.</p><p><strong>Results: </strong>TICCI is initiated by constructing a cell-neighborhood matrix using edge weights composed of intercellular similarity and CCI information. Louvain partitioning identifies trajectory branches, attenuating noise, while single-cell entropy (scEntropy) is used to assess differentiation status. The Chu-Liu algorithm constructs a directed least-square model to identify trajectory branches, and an improved diffusion fitted time algorithm computes cell-fitted time in nonconnected topologies. TICCI validation on single-cell RNA sequencing (scRNA-seq) datasets confirms the accuracy of cell trajectories, aligning with genealogical branching and gene markers. Verification using extrinsic information labels demonstrates CCI information utility in enhancing accurate trajectory inference. A comparative analysis establishes TICCI proficiency in accurate temporal ordering.</p><p><strong>Availability and implementation: </strong>Source code and binaries freely available for download at https://github.com/mine41/TICCI, implemented in R (version 4.32) and Python (version 3.7.16) and supported on MS Windows. Authors ensure that the software is available for a full two years following publication.</p>\",\"PeriodicalId\":93899,\"journal\":{\"name\":\"Bioinformatics (Oxford, England)\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.4000,\"publicationDate\":\"2025-02-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11829803/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bioinformatics (Oxford, England)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/bioinformatics/btaf027\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioinformatics (Oxford, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/bioinformatics/btaf027","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Trajectory Inference with Cell-Cell Interactions (TICCI): intercellular communication improves the accuracy of trajectory inference methods.
Motivation: Understanding cell differentiation and development dynamics is key for single-cell transcriptome analysis. Current cell differentiation trajectory inference algorithms face challenges such as high dimensionality, noise, and a need for users to possess certain biological information about the datasets to effectively utilize the algorithms. Here, we introduce Trajectory Inference with Cell-Cell Interaction (TICCI), a novel way to address these challenges by integrating intercellular communication information. In recognizing crucial intercellular communication during development, TICCI proposes Cell-Cell Interactions (CCI) at single-cell resolution. We posit that cells exhibiting higher gene expression similarity patterns are more likely to exchange information via biomolecular mediators.
Results: TICCI is initiated by constructing a cell-neighborhood matrix using edge weights composed of intercellular similarity and CCI information. Louvain partitioning identifies trajectory branches, attenuating noise, while single-cell entropy (scEntropy) is used to assess differentiation status. The Chu-Liu algorithm constructs a directed least-square model to identify trajectory branches, and an improved diffusion fitted time algorithm computes cell-fitted time in nonconnected topologies. TICCI validation on single-cell RNA sequencing (scRNA-seq) datasets confirms the accuracy of cell trajectories, aligning with genealogical branching and gene markers. Verification using extrinsic information labels demonstrates CCI information utility in enhancing accurate trajectory inference. A comparative analysis establishes TICCI proficiency in accurate temporal ordering.
Availability and implementation: Source code and binaries freely available for download at https://github.com/mine41/TICCI, implemented in R (version 4.32) and Python (version 3.7.16) and supported on MS Windows. Authors ensure that the software is available for a full two years following publication.