• 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

基于惩罚稳健分歧的基因-环境交互作用识别。

Gene-environment interaction identification via penalized robust divergence.

机构信息

School of Mathematics Sciences, University of Chinese Academy of Sciences, Beijing, P. R. China.

Key Laboratory of Big Data Mining and Knowledge Management, Chinese Academy of Sciences, Beijing, P. R. China.

出版信息

Biom J. 2022 Mar;64(3):461-480. doi: 10.1002/bimj.202000157. Epub 2021 Nov 1.

DOI:10.1002/bimj.202000157
PMID:34725857
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9386692/
Abstract

In high-throughput cancer studies, gene-environment interactions associated with outcomes have important implications. Some commonly adopted identification methods do not respect the "main effect, interaction" hierarchical structure. In addition, they can be challenged by data contamination and/or long-tailed distributions, which are not uncommon. In this article, robust methods based on -divergence and density power divergence are proposed to accommodate contaminated data/long-tailed distributions. A hierarchical sparse group penalty is adopted for regularized estimation and selection and can identify important gene-environment interactions and respect the "main effect, interaction" hierarchical structure. The proposed methods are implemented using an effective group coordinate descent algorithm. Simulation shows that when contamination occurs, the proposed methods can significantly outperform the existing alternatives with more accurate identification. The proposed approach is applied to the analysis of The Cancer Genome Atlas (TCGA) triple-negative breast cancer data and Gene Environment Association Studies (GENEVA) Type 2 Diabetes data.

摘要

在高通量癌症研究中,与结局相关的基因-环境相互作用具有重要意义。一些常用的识别方法不尊重“主效应,交互”层次结构。此外,它们可能会受到数据污染和/或长尾分布的挑战,这并不罕见。本文提出了基于 -散度和密度幂散度的稳健方法来适应污染数据/长尾分布。采用层次稀疏组惩罚进行正则化估计和选择,可以识别重要的基因-环境相互作用,并尊重“主效应,交互”层次结构。所提出的方法使用有效的组坐标下降算法实现。仿真表明,当发生污染时,所提出的方法可以通过更准确的识别显著优于现有替代方法。所提出的方法应用于分析癌症基因组图谱(TCGA)三阴性乳腺癌数据和基因环境关联研究(GENEVA)2 型糖尿病数据。

相似文献

1
Gene-environment interaction identification via penalized robust divergence.基于惩罚稳健分歧的基因-环境交互作用识别。
Biom J. 2022 Mar;64(3):461-480. doi: 10.1002/bimj.202000157. Epub 2021 Nov 1.
2
Dissecting gene-environment interactions: A penalized robust approach accounting for hierarchical structures.剖析基因-环境交互作用:一种考虑层次结构的惩罚稳健方法。
Stat Med. 2018 Feb 10;37(3):437-456. doi: 10.1002/sim.7518. Epub 2017 Oct 16.
3
A penalized robust semiparametric approach for gene-environment interactions.一种用于基因-环境相互作用的惩罚稳健半参数方法。
Stat Med. 2015 Dec 30;34(30):4016-30. doi: 10.1002/sim.6609. Epub 2015 Aug 3.
4
Robust semiparametric gene-environment interaction analysis using sparse boosting.使用稀疏提升进行稳健的半参数基因-环境交互作用分析。
Stat Med. 2019 Oct 15;38(23):4625-4641. doi: 10.1002/sim.8322. Epub 2019 Jul 29.
5
A penalized robust method for identifying gene-environment interactions.一种用于识别基因-环境交互作用的惩罚稳健方法。
Genet Epidemiol. 2014 Apr;38(3):220-30. doi: 10.1002/gepi.21795. Epub 2014 Feb 24.
6
Identifying gene-environment interactions for prognosis using a robust approach.使用稳健的方法识别基因-环境相互作用以进行预后评估。
Econom Stat. 2017 Oct;4:105-120. doi: 10.1016/j.ecosta.2016.10.004. Epub 2016 Nov 16.
7
Identification of gene-environment interactions in cancer studies using penalization.利用惩罚方法鉴定癌症研究中的基因-环境交互作用。
Genomics. 2013 Oct;102(4):189-94. doi: 10.1016/j.ygeno.2013.08.006. Epub 2013 Aug 29.
8
Inferring gene regulatory relationships with a high-dimensional robust approach.使用高维稳健方法推断基因调控关系。
Genet Epidemiol. 2017 Jul;41(5):437-454. doi: 10.1002/gepi.22047. Epub 2017 May 2.
9
Robust analysis of cancer heterogeneity for high-dimensional data.高维数据中癌症异质性的稳健分析。
Stat Med. 2022 Nov 30;41(27):5448-5462. doi: 10.1002/sim.9578. Epub 2022 Sep 18.
10
Robust Bayesian variable selection for gene-environment interactions.稳健的贝叶斯基因-环境交互作用变量选择。
Biometrics. 2023 Jun;79(2):684-694. doi: 10.1111/biom.13670. Epub 2022 Apr 16.

引用本文的文献

1
High-Dimensional Gene-Environment Interaction Analysis.高维基因-环境相互作用分析
Annu Rev Stat Appl. 2025 Mar;12. doi: 10.1146/annurev-statistics-112723-034315. Epub 2024 Sep 11.
2
Mutual-assistance learning for trustworthy biomarker discovery and disease prediction.用于可靠生物标志物发现和疾病预测的互助学习。
Brief Bioinform. 2025 Mar 4;26(2). doi: 10.1093/bib/bbaf178.
3
Springer: An R package for bi-level variable selection of high-dimensional longitudinal data.施普林格:用于高维纵向数据双层变量选择的R包。

本文引用的文献

1
Exploring specific prognostic biomarkers in triple-negative breast cancer.探索三阴性乳腺癌中的特定预后生物标志物。
Cell Death Dis. 2019 Oct 24;10(11):807. doi: 10.1038/s41419-019-2043-x.
2
Identification of potential key genes and pathways predicting pathogenesis and prognosis for triple-negative breast cancer.预测三阴性乳腺癌发病机制和预后的潜在关键基因及通路的鉴定
Cancer Cell Int. 2019 Jun 28;19:172. doi: 10.1186/s12935-019-0884-0. eCollection 2019.
3
High genetic risk scores of SLIT3, PLEKHA5 and PPP2R2C variants increased insulin resistance and interacted with coffee and caffeine consumption in middle-aged adults.
Front Genet. 2023 Apr 6;14:1088223. doi: 10.3389/fgene.2023.1088223. eCollection 2023.
4
Interep: An R Package for High-Dimensional Interaction Analysis of the Repeated Measurement Data.Interep:一个用于重复测量数据高维交互分析的R软件包。
Genes (Basel). 2022 Mar 19;13(3):544. doi: 10.3390/genes13030544.
SLIT3、PLEKHA5和PPP2R2C变异体的高遗传风险评分增加了中年成年人的胰岛素抵抗,并与咖啡和咖啡因的摄入量相互作用。
Nutr Metab Cardiovasc Dis. 2019 Jan;29(1):79-89. doi: 10.1016/j.numecd.2018.09.009. Epub 2018 Sep 28.
4
DNA Methylation Predicts the Response of Triple-Negative Breast Cancers to All-Trans Retinoic Acid.DNA甲基化可预测三阴性乳腺癌对全反式维甲酸的反应。
Cancers (Basel). 2018 Oct 24;10(11):397. doi: 10.3390/cancers10110397.
5
Epigenetic activation of HORMAD1 in basal-like breast cancer: role in Rucaparib sensitivity.激素相关蛋白1(HORMAD1)在基底样乳腺癌中的表观遗传激活:在鲁卡帕尼敏感性中的作用
Oncotarget. 2018 Jul 10;9(53):30115-30127. doi: 10.18632/oncotarget.25728.
6
Robust genetic interaction analysis.稳健的遗传交互作用分析。
Brief Bioinform. 2019 Mar 25;20(2):624-637. doi: 10.1093/bib/bby033.
7
Ensemble outlier detection and gene selection in triple-negative breast cancer data.三阴性乳腺癌数据中的集成异常值检测和基因选择。
BMC Bioinformatics. 2018 May 4;19(1):168. doi: 10.1186/s12859-018-2149-7.
8
Guideline Summary: American Society of Clinical Oncology/College of American Pathologists Guideline Recommendations for Human Epidermal Growth Factor Receptor HER2 Testing in Breast Cancer.指南摘要:美国临床肿瘤学会/美国病理学家学会关于乳腺癌中人表皮生长因子受体HER2检测的指南建议
J Oncol Pract. 2007 Jan;3(1):48-50. doi: 10.1200/JOP.0718501.
9
Virtual Screening and Prediction of Binding of Caprine CSN1S2 Protein Tryptic Peptides to Glucokinase.山羊CSN1S2蛋白胰蛋白酶肽段与葡萄糖激酶结合的虚拟筛选及预测
Acta Inform Med. 2017 Dec;25(4):225-231. doi: 10.5455/aim.2017.25.225-231.
10
Dissecting gene-environment interactions: A penalized robust approach accounting for hierarchical structures.剖析基因-环境交互作用:一种考虑层次结构的惩罚稳健方法。
Stat Med. 2018 Feb 10;37(3):437-456. doi: 10.1002/sim.7518. Epub 2017 Oct 16.