• 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

基因先驱:一个用于识别癌症中必需基因和模块的综合Python软件包。

GenePioneer: a comprehensive Python package for identification of essential genes and modules in cancer.

作者信息

Haerianardakani Amirhossein, Taheri Golnaz

机构信息

Department of Computer and Systems Sciences, Stockholm University, Stockholm 16455, Sweden.

School of Electrical Engineering and Computer Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm 10044, Sweden.

出版信息

Bioinform Adv. 2025 Apr 29;5(1):vbaf094. doi: 10.1093/bioadv/vbaf094. eCollection 2025.

DOI:10.1093/bioadv/vbaf094
PMID:40417653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12098931/
Abstract

SUMMARY

We propose a network-based unsupervised learning model to identify essential cancer genes and modules for 12 different cancer types, supported by a Python package for practical application. The model constructs a gene network from frequently mutated genes and biological processes, ranks genes using topological features, and detects critical modules. Evaluation across cancer types confirms its effectiveness in prioritizing cancer-related genes and uncovering relevant modules. The Python package allows users to input gene lists, retrieve rankings, and identify associated modules. This work provides a robust method for gene prioritization and module detection, along with a user-friendly package to support research and clinical decision-making in cancer genomics.

AVAILABILITY AND IMPLEMENTATION

GenePioneer is released as an open-source software under the MIT license. The source code is available on GitHub at https://github.com/Golnazthr/ModuleDetection.

摘要

摘要

我们提出了一种基于网络的无监督学习模型,用于识别12种不同癌症类型的关键癌症基因和模块,并提供了一个用于实际应用的Python包。该模型从频繁突变的基因和生物学过程构建基因网络,利用拓扑特征对基因进行排名,并检测关键模块。跨癌症类型的评估证实了其在对癌症相关基因进行优先级排序和发现相关模块方面的有效性。该Python包允许用户输入基因列表、检索排名并识别相关模块。这项工作为基因优先级排序和模块检测提供了一种强大的方法,以及一个用户友好的包,以支持癌症基因组学的研究和临床决策。

可用性和实现方式

GenePioneer作为开源软件根据MIT许可发布。源代码可在GitHub上获取,网址为https://github.com/Golnazthr/ModuleDetection 。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2141/12098931/e639a4b111a5/vbaf094f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2141/12098931/ff77ca5ba320/vbaf094f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2141/12098931/41185239e690/vbaf094f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2141/12098931/e639a4b111a5/vbaf094f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2141/12098931/ff77ca5ba320/vbaf094f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2141/12098931/41185239e690/vbaf094f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2141/12098931/e639a4b111a5/vbaf094f3.jpg

相似文献

1
GenePioneer: a comprehensive Python package for identification of essential genes and modules in cancer.基因先驱:一个用于识别癌症中必需基因和模块的综合Python软件包。
Bioinform Adv. 2025 Apr 29;5(1):vbaf094. doi: 10.1093/bioadv/vbaf094. eCollection 2025.
2
Molecular feature-based classification of retroperitoneal liposarcoma: a prospective cohort study.基于分子特征的腹膜后脂肪肉瘤分类:一项前瞻性队列研究。
Elife. 2025 May 23;14:RP100887. doi: 10.7554/eLife.100887.
3
rPIMS: a ShinyR package for the precision identification and modelling of livestock breeds using genomic data and machine learning approaches.rPIMS:一个用于利用基因组数据和机器学习方法对家畜品种进行精准识别和建模的ShinyR软件包。
Bioinform Adv. 2025 Apr 7;5(1):vbaf077. doi: 10.1093/bioadv/vbaf077. eCollection 2025.
4
Assessing the comparative effects of interventions in COPD: a tutorial on network meta-analysis for clinicians.评估慢性阻塞性肺疾病干预措施的比较效果:面向临床医生的网状Meta分析教程
Respir Res. 2024 Dec 21;25(1):438. doi: 10.1186/s12931-024-03056-x.
5
DiSC: a statistical tool for fast differential expression analysis of individual-level single-cell RNA-seq data.DiSC:一种用于个体水平单细胞RNA测序数据快速差异表达分析的统计工具。
Bioinformatics. 2025 Jun 2;41(6). doi: 10.1093/bioinformatics/btaf327.
6
Feasibility study of Learning Together for Mental Health: fidelity, reach and acceptability of a whole-school intervention aiming to promote health and wellbeing in secondary schools.“共同学习促进心理健康”可行性研究:一项旨在促进中学健康与幸福的全校性干预措施的保真度、覆盖面和可接受性。
Public Health Res (Southampt). 2025 Jun 18:1-36. doi: 10.3310/RTRT0202.
7
Development of a machine learning model and a web application for predicting neurological outcome at hospital discharge in spinal cord injury patients.开发用于预测脊髓损伤患者出院时神经功能结局的机器学习模型和网络应用程序。
Spine J. 2025 Jan 31. doi: 10.1016/j.spinee.2025.01.005.
8
XeroGraph: enhancing data integrity in the presence of missing values with statistical and predictive analysis.XeroGraph:通过统计和预测分析在存在缺失值的情况下增强数据完整性。
Bioinform Adv. 2025 Feb 21;5(1):vbaf035. doi: 10.1093/bioadv/vbaf035. eCollection 2025.
9
Stakeholders' perceptions and experiences of factors influencing the commissioning, delivery, and uptake of general health checks: a qualitative evidence synthesis.利益相关者对影响一般健康检查的委托、提供和接受因素的看法与体验:一项定性证据综合分析
Cochrane Database Syst Rev. 2025 Mar 20;3(3):CD014796. doi: 10.1002/14651858.CD014796.pub2.
10
Electronic cigarettes for smoking cessation.用于戒烟的电子烟。
Cochrane Database Syst Rev. 2025 Jan 29;1(1):CD010216. doi: 10.1002/14651858.CD010216.pub9.

本文引用的文献

1
Uncovering driver genes in breast cancer through an innovative machine learning mutational analysis method.通过创新的机器学习突变分析方法揭示乳腺癌的驱动基因。
Comput Biol Med. 2024 Mar;171:108234. doi: 10.1016/j.compbiomed.2024.108234. Epub 2024 Feb 29.
2
A new machine learning method for cancer mutation analysis.一种用于癌症基因突变分析的新机器学习方法。
PLoS Comput Biol. 2022 Oct 17;18(10):e1010332. doi: 10.1371/journal.pcbi.1010332. eCollection 2022 Oct.
3
Comprehensive analysis of pathways in Coronavirus 2019 (COVID-19) using an unsupervised machine learning method.
使用无监督机器学习方法对2019冠状病毒病(COVID-19)中的通路进行综合分析。
Appl Soft Comput. 2022 Oct;128:109510. doi: 10.1016/j.asoc.2022.109510. Epub 2022 Aug 17.
4
The Gene Ontology Resource: 20 years and still GOing strong.《基因本体论资源:20 年,持续强大》
Nucleic Acids Res. 2019 Jan 8;47(D1):D330-D338. doi: 10.1093/nar/gky1055.
5
UniProt: a worldwide hub of protein knowledge.UniProt:蛋白质知识的全球枢纽。
Nucleic Acids Res. 2019 Jan 8;47(D1):D506-D515. doi: 10.1093/nar/gky1049.
6
Tumour heterogeneity and resistance to cancer therapies.肿瘤异质性与癌症治疗耐药性。
Nat Rev Clin Oncol. 2018 Feb;15(2):81-94. doi: 10.1038/nrclinonc.2017.166. Epub 2017 Nov 8.
7
KEGG as a reference resource for gene and protein annotation.KEGG作为基因和蛋白质注释的参考资源。
Nucleic Acids Res. 2016 Jan 4;44(D1):D457-62. doi: 10.1093/nar/gkv1070. Epub 2015 Oct 17.
8
Discovery and saturation analysis of cancer genes across 21 tumour types.在 21 种肿瘤类型中发现和饱和分析癌症基因。
Nature. 2014 Jan 23;505(7484):495-501. doi: 10.1038/nature12912. Epub 2014 Jan 5.
9
Rate, molecular spectrum, and consequences of human mutation.人类突变的速率、分子谱和后果。
Proc Natl Acad Sci U S A. 2010 Jan 19;107(3):961-8. doi: 10.1073/pnas.0912629107. Epub 2010 Jan 4.
10
Comprehensive genomic characterization defines human glioblastoma genes and core pathways.全面的基因组特征分析确定了人类胶质母细胞瘤的基因和核心通路。
Nature. 2008 Oct 23;455(7216):1061-8. doi: 10.1038/nature07385. Epub 2008 Sep 4.