• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

scCTS:从群体水平的单细胞 RNA-seq 中识别细胞类型特异性标记基因。

scCTS: identifying the cell type-specific marker genes from population-level single-cell RNA-seq.

机构信息

Department of Biostatistics and Bioinformatics, Emory University, Atlanta, GA, 30322, USA.

School of Data Science, The Chinese University of Hong Kong, Shenzhen (CUHK-SZ), Shenzhen, 518172, Guangdong, China.

出版信息

Genome Biol. 2024 Oct 14;25(1):269. doi: 10.1186/s13059-024-03410-8.

DOI:10.1186/s13059-024-03410-8
PMID:39402623
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11472465/
Abstract

Single-cell RNA-sequencing (scRNA-seq) provides gene expression profiles of individual cells from complex samples, facilitating the detection of cell type-specific marker genes. In scRNA-seq experiments with multiple donors, the population level variation brings an extra layer of complexity in cell type-specific gene detection, for example, they may not appear in all donors. Motivated by this observation, we develop a statistical model named scCTS to identify cell type-specific genes from population-level scRNA-seq data. Extensive data analyses demonstrate that the proposed method identifies more biologically meaningful cell type-specific genes compared to traditional methods.

摘要

单细胞 RNA 测序 (scRNA-seq) 为复杂样本中的单个细胞提供基因表达谱,有助于检测细胞类型特异性标记基因。在具有多个供体的 scRNA-seq 实验中,群体水平的变异给细胞类型特异性基因检测带来了额外的复杂性,例如,它们可能不会出现在所有供体中。受此观察结果的启发,我们开发了一种名为 scCTS 的统计模型,用于从群体水平的 scRNA-seq 数据中识别细胞类型特异性基因。广泛的数据分析表明,与传统方法相比,该方法可以识别出更具生物学意义的细胞类型特异性基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/a4ca57c17d74/13059_2024_3410_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/c952de705de5/13059_2024_3410_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/99a067ef9ad7/13059_2024_3410_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/519d0785ee56/13059_2024_3410_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/268374665ed5/13059_2024_3410_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/a4ca57c17d74/13059_2024_3410_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/c952de705de5/13059_2024_3410_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/99a067ef9ad7/13059_2024_3410_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/519d0785ee56/13059_2024_3410_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/268374665ed5/13059_2024_3410_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db62/11472465/a4ca57c17d74/13059_2024_3410_Fig5_HTML.jpg

相似文献

1
scCTS: identifying the cell type-specific marker genes from population-level single-cell RNA-seq.scCTS:从群体水平的单细胞 RNA-seq 中识别细胞类型特异性标记基因。
Genome Biol. 2024 Oct 14;25(1):269. doi: 10.1186/s13059-024-03410-8.
2
Identifying cell states in single-cell RNA-seq data at statistically maximal resolution.以统计学上最大分辨率识别单细胞 RNA-seq 数据中的细胞状态。
PLoS Comput Biol. 2024 Jul 12;20(7):e1012224. doi: 10.1371/journal.pcbi.1012224. eCollection 2024 Jul.
3
A Comprehensive Survey of Statistical Approaches for Differential Expression Analysis in Single-Cell RNA Sequencing Studies.单细胞 RNA 测序研究中差异表达分析的统计方法综合综述。
Genes (Basel). 2021 Dec 2;12(12):1947. doi: 10.3390/genes12121947.
4
A robust model for cell type-specific interindividual variation in single-cell RNA sequencing data.单细胞 RNA 测序数据中细胞类型特异性个体间变异的稳健模型。
Nat Commun. 2024 Jun 19;15(1):5229. doi: 10.1038/s41467-024-49242-9.
5
XgCPred: Cell type classification using XGBoost-CNN integration and exploiting gene expression imaging in single-cell RNAseq data.XgCPred:基于 XGBoost-CNN 集成和单细胞 RNAseq 数据中基因表达成像的细胞类型分类。
Comput Biol Med. 2024 Oct;181:109066. doi: 10.1016/j.compbiomed.2024.109066. Epub 2024 Aug 24.
6
Model-based deep embedding for constrained clustering analysis of single cell RNA-seq data.基于模型的深度学习嵌入方法用于单细胞 RNA-seq 数据的约束聚类分析。
Nat Commun. 2021 Mar 25;12(1):1873. doi: 10.1038/s41467-021-22008-3.
7
scDMAE: A Generative Denoising Model Adopted Mask Strategy for scRNA-Seq Data Recovery.scDMAE:一种采用掩模策略的生成去噪模型,用于 scRNA-Seq 数据恢复。
IEEE J Biomed Health Inform. 2024 Jun;28(6):3772-3780. doi: 10.1109/JBHI.2024.3383921. Epub 2024 Jun 6.
8
Using RNentropy to Detect Significant Variation in Gene Expression Across Multiple RNA-Seq or Single-Cell RNA-Seq Samples.使用 RNentropy 检测多个 RNA-Seq 或单细胞 RNA-Seq 样本中基因表达的显著变化。
Methods Mol Biol. 2021;2284:77-96. doi: 10.1007/978-1-0716-1307-8_6.
9
Bubble: a fast single-cell RNA-seq imputation using an autoencoder constrained by bulk RNA-seq data.Bubble:一种利用受批量RNA测序数据约束的自动编码器进行的快速单细胞RNA测序插补方法。
Brief Bioinform. 2023 Jan 19;24(1). doi: 10.1093/bib/bbac580.
10
Collaborative Structure-Preserved Missing Data Imputation for Single-Cell RNA-Seq Clustering.单细胞 RNA-Seq 聚类的协作结构保留缺失数据插补。
IEEE/ACM Trans Comput Biol Bioinform. 2024 Sep-Oct;21(5):1480-1491. doi: 10.1109/TCBB.2024.3404013. Epub 2024 Oct 9.

引用本文的文献

1
Reference-free deconvolution of complex samples based on cross-cell-type differential analysis: Systematic evaluations with various feature selection options.基于跨细胞类型差异分析的复杂样本无参考去卷积:使用各种特征选择选项的系统评估
Front Genet. 2025 May 30;16:1570781. doi: 10.3389/fgene.2025.1570781. eCollection 2025.
2
Long noncoding RNAs in familial hypercholesterolemia: biomarkers, therapeutics, and AI in precision medicine.家族性高胆固醇血症中的长链非编码RNA:精准医学中的生物标志物、治疗方法及人工智能
Lipids Health Dis. 2025 May 21;24(1):182. doi: 10.1186/s12944-025-02605-7.

本文引用的文献

1
imply: improving cell-type deconvolution accuracy using personalized reference profiles.提示:使用个性化参考图谱提高细胞类型去卷积准确性。
Genome Med. 2024 Apr 29;16(1):65. doi: 10.1186/s13073-024-01338-z.
2
Uncovering cell identity through differential stability with Cepo.利用Cepo通过差异稳定性揭示细胞身份。
Nat Comput Sci. 2021 Dec;1(12):784-790. doi: 10.1038/s43588-021-00172-2. Epub 2021 Dec 20.
3
Population-level integration of single-cell datasets enables multi-scale analysis across samples.单细胞数据集的群体水平整合能够实现跨样本的多尺度分析。
Nat Methods. 2023 Nov;20(11):1683-1692. doi: 10.1038/s41592-023-02035-2. Epub 2023 Oct 9.
4
Atlas-scale single-cell multi-sample multi-condition data integration using scMerge2.使用 scMerge2 进行图谱尺度单细胞多样本多条件数据整合。
Nat Commun. 2023 Jul 17;14(1):4272. doi: 10.1038/s41467-023-39923-2.
5
Debiased personalized gene coexpression networks for population-scale scRNA-seq data.基于去偏置的个性化基因共表达网络的人群规模 scRNA-seq 数据分析。
Genome Res. 2023 Jun;33(6):932-947. doi: 10.1101/gr.277363.122. Epub 2023 Jun 9.
6
A machine learning-based method for automatically identifying novel cells in annotating single-cell RNA-seq data.基于机器学习的方法,用于自动识别注释单细胞 RNA-seq 数据中的新型细胞。
Bioinformatics. 2022 Oct 31;38(21):4885-4892. doi: 10.1093/bioinformatics/btac617.
7
Unsupervised cell functional annotation for single-cell RNA-seq.无监督的单细胞 RNA-seq 细胞功能注释。
Genome Res. 2022 Sep 27;32(9):1765-1775. doi: 10.1101/gr.276609.122.
8
Cell Type-Specific Induction of Inflammation-Associated Genes in Crohn's Disease and Colorectal Cancer.细胞类型特异性诱导炎症相关基因在克罗恩病和结直肠癌。
Int J Mol Sci. 2022 Mar 12;23(6):3082. doi: 10.3390/ijms23063082.
9
scGate: marker-based purification of cell types from heterogeneous single-cell RNA-seq datasets.scGate:基于标记的异质单细胞 RNA-seq 数据集细胞类型的纯化。
Bioinformatics. 2022 Apr 28;38(9):2642-2644. doi: 10.1093/bioinformatics/btac141.
10
splatPop: simulating population scale single-cell RNA sequencing data.splatPop:模拟群体规模单细胞 RNA 测序数据。
Genome Biol. 2021 Dec 15;22(1):341. doi: 10.1186/s13059-021-02546-1.