• 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

评估抽样偏差对合成网络和生物网络中节点中心性的影响。

Assessing the impact of sampling bias on node centralities in synthetic and biological networks.

作者信息

Salehzadeh-Yazdi Ali, Hütt Marc-Thorsten

机构信息

School of Science, Constructor University, Bremen, Germany.

出版信息

NPJ Syst Biol Appl. 2025 May 15;11(1):47. doi: 10.1038/s41540-025-00526-w.

DOI:10.1038/s41540-025-00526-w
PMID:40374666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12081662/
Abstract

Centrality measures are crucial for network analysis, offering insights into node importance within complex networks. However, their accuracy is often affected by observational errors and incomplete data. This study investigates how sampling biases systematically impact centrality measures. We simulate six types of biased down-sampling, transitioning networks from dense to sparse states, using the initial network as the 'ground truth.' Changes in centrality values reveal the robustness of these measures under various sampling scenarios across synthetic and biological networks. Our results show that in synthetic networks, some sampling methods consistently exhibit higher robustness, particularly in scale-free networks. For biological networks, protein interaction networks are the most robust, followed by metabolite, gene regulatory, and reaction networks. Local centrality measures generally show greater robustness, while global measures are more heterogeneous and less reliable. This study highlights the limitations of centrality measures under sampling biases and informs the development of more robust methodologies.

摘要

中心性度量对于网络分析至关重要,它能深入了解复杂网络中节点的重要性。然而,其准确性常常受到观测误差和不完整数据的影响。本研究调查了抽样偏差如何系统性地影响中心性度量。我们模拟了六种类型的有偏下采样,将网络从密集状态转变为稀疏状态,以初始网络作为“真实情况”。中心性值的变化揭示了这些度量在合成网络和生物网络的各种采样场景下的稳健性。我们的结果表明,在合成网络中,一些采样方法始终表现出更高的稳健性,尤其是在无标度网络中。对于生物网络,蛋白质相互作用网络最为稳健,其次是代谢物、基因调控和反应网络。局部中心性度量通常表现出更高的稳健性,而全局度量则更加参差不齐且可靠性较低。本研究突出了抽样偏差下中心性度量的局限性,并为更稳健方法的开发提供了参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/1d1eae36758d/41540_2025_526_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/df87a230eb1c/41540_2025_526_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/c598998903e9/41540_2025_526_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/861e81542800/41540_2025_526_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/a0480ef0b6b4/41540_2025_526_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/266b0ac6f428/41540_2025_526_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/978d8ca14ec4/41540_2025_526_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/1d1eae36758d/41540_2025_526_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/df87a230eb1c/41540_2025_526_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/c598998903e9/41540_2025_526_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/861e81542800/41540_2025_526_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/a0480ef0b6b4/41540_2025_526_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/266b0ac6f428/41540_2025_526_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/978d8ca14ec4/41540_2025_526_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aee/12081662/1d1eae36758d/41540_2025_526_Fig7_HTML.jpg

相似文献

1
Assessing the impact of sampling bias on node centralities in synthetic and biological networks.评估抽样偏差对合成网络和生物网络中节点中心性的影响。
NPJ Syst Biol Appl. 2025 May 15;11(1):47. doi: 10.1038/s41540-025-00526-w.
2
Clone temporal centrality measures for incomplete sequences of graph snapshots.针对图快照的不完整序列的克隆时间中心性度量。
BMC Bioinformatics. 2017 May 16;18(1):261. doi: 10.1186/s12859-017-1677-x.
3
Centralities in simplicial complexes. Applications to protein interaction networks.单纯复形中的中心性。在蛋白质相互作用网络中的应用。
J Theor Biol. 2018 Feb 7;438:46-60. doi: 10.1016/j.jtbi.2017.11.003. Epub 2017 Nov 8.
4
Exploration of biological network centralities with CentiBiN.使用CentiBiN探索生物网络中心性
BMC Bioinformatics. 2006 Apr 21;7:219. doi: 10.1186/1471-2105-7-219.
5
Measures of centrality based on the spectrum of the Laplacian.基于拉普拉斯谱的中心性度量。
Phys Rev E Stat Nonlin Soft Matter Phys. 2012 Jun;85(6 Pt 2):066127. doi: 10.1103/PhysRevE.85.066127. Epub 2012 Jun 20.
6
Assessing structural uncertainty of biochemical regulatory networks in metabolic pathways under varying data quality.评估代谢途径中生化调控网络在不同数据质量下的结构不确定性。
NPJ Syst Biol Appl. 2024 Aug 22;10(1):94. doi: 10.1038/s41540-024-00412-x.
7
Anti-triangle centrality-based community detection in complex networks.基于反三角中心度的复杂网络社区检测。
IET Syst Biol. 2014 Jun;8(3):116-25. doi: 10.1049/iet-syb.2013.0039.
8
Measuring rank robustness in scored protein interaction networks.测量有评分的蛋白质相互作用网络中的等级鲁棒性。
BMC Bioinformatics. 2019 Aug 28;20(1):446. doi: 10.1186/s12859-019-3036-6.
9
Generalized walks-based centrality measures for complex biological networks.基于广义游走的复杂生物网络中心性度量
J Theor Biol. 2010 Apr 21;263(4):556-65. doi: 10.1016/j.jtbi.2010.01.014. Epub 2010 Jan 18.
10
Systematic Approach to Computational Design of Gene Regulatory Networks with Information Processing Capabilities.具有信息处理能力的基因调控网络计算设计的系统方法。
IEEE/ACM Trans Comput Biol Bioinform. 2014 Mar-Apr;11(2):431-40. doi: 10.1109/TCBB.2013.2295792.

本文引用的文献

1
Topological benchmarking of algorithms to infer gene regulatory networks from single-cell RNA-seq data.从单细胞 RNA-seq 数据中推断基因调控网络的算法的拓扑基准测试。
Bioinformatics. 2024 May 2;40(5). doi: 10.1093/bioinformatics/btae267.
2
The STRING database in 2023: protein-protein association networks and functional enrichment analyses for any sequenced genome of interest.2023 年的 STRING 数据库:针对任何感兴趣的测序基因组的蛋白质-蛋白质关联网络和功能富集分析。
Nucleic Acids Res. 2023 Jan 6;51(D1):D638-D646. doi: 10.1093/nar/gkac1000.
3
Understudied proteins: opportunities and challenges for functional proteomics.
研究不足的蛋白质:功能蛋白质组学面临的机遇与挑战
Nat Methods. 2022 Jul;19(7):774-779. doi: 10.1038/s41592-022-01454-x.
4
Identifying influential spreaders in complex networks for disease spread and control.识别复杂网络中疾病传播和控制的有影响力的传播者。
Sci Rep. 2022 Apr 1;12(1):5550. doi: 10.1038/s41598-022-09341-3.
5
Three topological features of regulatory networks control life-essential and specialized subsystems.调控网络的三个拓扑特征控制着生命必需和特化的子系统。
Sci Rep. 2021 Dec 20;11(1):24209. doi: 10.1038/s41598-021-03625-w.
6
Assessing regulatory features of the current transcriptional network of Saccharomyces cerevisiae.评估酿酒酵母当前转录网络的调控特征。
Sci Rep. 2020 Oct 20;10(1):17744. doi: 10.1038/s41598-020-74043-7.
7
The BioGRID database: A comprehensive biomedical resource of curated protein, genetic, and chemical interactions.The BioGRID 数据库:一个经过精心整理的生物医学资源,包含蛋白质、遗传和化学相互作用。
Protein Sci. 2021 Jan;30(1):187-200. doi: 10.1002/pro.3978. Epub 2020 Nov 23.
8
GEMtractor: extracting views into genome-scale metabolic models.GEMtractor:将视图提取到基因组规模的代谢模型中。
Bioinformatics. 2020 May 1;36(10):3281-3282. doi: 10.1093/bioinformatics/btaa068.
9
YEASTRACT+: a portal for cross-species comparative genomics of transcription regulation in yeasts.YEASTRACT+:一个用于酵母转录调控的跨物种比较基因组学的门户。
Nucleic Acids Res. 2020 Jan 8;48(D1):D642-D649. doi: 10.1093/nar/gkz859.
10
Ranking Regions, Edges and Classifying Tasks in Functional Brain Graphs by Sub-Graph Entropy.基于子图摘熵对功能脑网络中的区域、边和任务进行排序和分类。
Sci Rep. 2019 May 20;9(1):7628. doi: 10.1038/s41598-019-44103-8.