• 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

相似文献

1
A Hierarchical Approach Using Marginal Summary Statistics for Multiple Intermediates in a Mendelian Randomization or Transcriptome Analysis.基于边缘汇总统计量的分层方法在孟德尔随机化或转录组分析中用于多个中介。
Am J Epidemiol. 2021 Jun 1;190(6):1148-1158. doi: 10.1093/aje/kwaa287.
2
Hierarchical joint analysis of marginal summary statistics-Part II: High-dimensional instrumental analysis of omics data.边际汇总统计量的分层联合分析 - 第二部分:组学数据的高维工具变量分析
Genet Epidemiol. 2024 Oct;48(7):291-309. doi: 10.1002/gepi.22577. Epub 2024 Jun 17.
3
Genetically proxied glucose-lowering drug target perturbation and risk of cancer: a Mendelian randomisation analysis.基于遗传关联的降糖药物靶点干预与癌症风险:一项孟德尔随机化分析。
Diabetologia. 2023 Aug;66(8):1481-1500. doi: 10.1007/s00125-023-05925-4. Epub 2023 May 12.
4
Inferring causal direction between two traits using R with application to transcriptome-wide association studies.使用 R 推断两个性状之间的因果关系及其在转录组关联研究中的应用。
Am J Hum Genet. 2024 Aug 8;111(8):1782-1795. doi: 10.1016/j.ajhg.2024.06.013. Epub 2024 Jul 24.
5
Multivariable MR Can Mitigate Bias in Two-Sample MR Using Covariable-Adjusted Summary Associations.多变量孟德尔随机化可以利用协变量调整后的汇总关联来减轻两样本孟德尔随机化中的偏差。
Genet Epidemiol. 2025 Jan;49(1):e22606. doi: 10.1002/gepi.22606.
6
Model checking via testing for direct effects in Mendelian Randomization and transcriptome-wide association studies.基于孟德尔随机化和转录组关联研究中直接效应的检验进行模型检测。
PLoS Comput Biol. 2021 Aug 2;17(8):e1009266. doi: 10.1371/journal.pcbi.1009266. eCollection 2021 Aug.
7
Association of organ iron levels with type 2 diabetes mellitus and glycemic traits: A bidirectional two-sample Mendelian randomization study.器官铁水平与2型糖尿病及血糖特征的关联:一项双向双样本孟德尔随机化研究
J Trace Elem Med Biol. 2025 Feb;87:127586. doi: 10.1016/j.jtemb.2024.127586. Epub 2024 Dec 27.
8
Multi-trait transcriptome-wide association studies with probabilistic Mendelian randomization.多性状全转录组关联研究与概率性孟德尔随机化。
Am J Hum Genet. 2021 Feb 4;108(2):240-256. doi: 10.1016/j.ajhg.2020.12.006.
9
Unbiased causal inference with Mendelian randomization and covariate-adjusted GWAS data.利用孟德尔随机化和协变量调整的全基因组关联研究数据进行无偏因果推断。
HGG Adv. 2025 Apr 10;6(2):100412. doi: 10.1016/j.xhgg.2025.100412. Epub 2025 Jan 30.
10
Drug-target Mendelian randomization revealed a significant association of genetically proxied metformin effects with increased prostate cancer risk.药物靶点孟德尔随机化研究表明,遗传上接近二甲双胍作用的药物与前列腺癌风险增加显著相关。
Mol Carcinog. 2024 May;63(5):849-858. doi: 10.1002/mc.23692. Epub 2024 Mar 22.

引用本文的文献

1
The goldmine of GWAS summary statistics: a systematic review of methods and tools.全基因组关联研究汇总统计数据的宝库:方法与工具的系统综述
BioData Min. 2024 Sep 5;17(1):31. doi: 10.1186/s13040-024-00385-x.
2
Hierarchical joint analysis of marginal summary statistics-Part II: High-dimensional instrumental analysis of omics data.边际汇总统计量的分层联合分析 - 第二部分:组学数据的高维工具变量分析
Genet Epidemiol. 2024 Oct;48(7):291-309. doi: 10.1002/gepi.22577. Epub 2024 Jun 17.
3
Hierarchical joint analysis of marginal summary statistics-Part I: Multipopulation fine mapping and credible set construction.分层联合边缘汇总统计量分析 - 第一部分:多群体精细映射和可信集构建。
Genet Epidemiol. 2024 Sep;48(6):241-257. doi: 10.1002/gepi.22562. Epub 2024 Apr 12.
4
Mendelian randomization.孟德尔随机化
Nat Rev Methods Primers. 2022 Feb 10;2. doi: 10.1038/s43586-021-00092-5.
5
Statistical methods for cis-Mendelian randomization with two-sample summary-level data.基于两样本汇总数据的顺式孟德尔随机化的统计方法。
Genet Epidemiol. 2023 Feb;47(1):3-25. doi: 10.1002/gepi.22506. Epub 2022 Oct 23.

本文引用的文献

1
Bayesian variable selection with a pleiotropic loss function in Mendelian randomization.贝叶斯变量选择与孟德尔随机化中的多效性损失函数。
Stat Med. 2021 Oct 15;40(23):5025-5045. doi: 10.1002/sim.9109. Epub 2021 Jun 21.
2
How humans can contribute to Mendelian randomization analyses.人类如何为孟德尔随机化分析做出贡献。
Int J Epidemiol. 2019 Jun 1;48(3):661-664. doi: 10.1093/ije/dyz152.
3
Identification of Novel Susceptibility Loci and Genes for Prostate Cancer Risk: A Transcriptome-Wide Association Study in Over 140,000 European Descendants.鉴定前列腺癌风险的新易感性基因座和基因:超过 14 万欧洲后裔的转录组关联研究。
Cancer Res. 2019 Jul 1;79(13):3192-3204. doi: 10.1158/0008-5472.CAN-18-3536. Epub 2019 May 17.
4
Fast and flexible linear mixed models for genome-wide genetics.快速灵活的全基因组遗传学线性混合模型。
PLoS Genet. 2019 Feb 8;15(2):e1007978. doi: 10.1371/journal.pgen.1007978. eCollection 2019 Feb.
5
An examination of multivariable Mendelian randomization in the single-sample and two-sample summary data settings.多变量孟德尔随机化在单样本和两样本汇总数据设置中的检验。
Int J Epidemiol. 2019 Jun 1;48(3):713-727. doi: 10.1093/ije/dyy262.
6
Large-scale transcriptome-wide association study identifies new prostate cancer risk regions.大规模转录组全基因组关联研究鉴定出新的前列腺癌风险区域。
Nat Commun. 2018 Oct 4;9(1):4079. doi: 10.1038/s41467-018-06302-1.
7
Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes.全基因组关联分析鉴定出 143 个 2 型糖尿病风险变异和潜在调控机制。
Nat Commun. 2018 Jul 27;9(1):2941. doi: 10.1038/s41467-018-04951-w.
8
Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci.对超过 14 万名男性的关联分析确定了 63 个新的前列腺癌易感性位点。
Nat Genet. 2018 Jul;50(7):928-936. doi: 10.1038/s41588-018-0142-8. Epub 2018 Jun 11.
9
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.从 GWAS 汇总统计数据推断组织特异性基因表达变异的表型后果。
Nat Commun. 2018 May 8;9(1):1825. doi: 10.1038/s41467-018-03621-1.
10
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases.检测复杂性状和疾病之间的孟德尔随机化因果关系推断中广泛存在的水平 pleiotropy。
Nat Genet. 2018 May;50(5):693-698. doi: 10.1038/s41588-018-0099-7. Epub 2018 Apr 23.

基于边缘汇总统计量的分层方法在孟德尔随机化或转录组分析中用于多个中介。

A Hierarchical Approach Using Marginal Summary Statistics for Multiple Intermediates in a Mendelian Randomization or Transcriptome Analysis.

出版信息

Am J Epidemiol. 2021 Jun 1;190(6):1148-1158. doi: 10.1093/aje/kwaa287.

DOI:10.1093/aje/kwaa287
PMID:33404048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8521785/
Abstract

Previous research has demonstrated the usefulness of hierarchical modeling for incorporating a flexible array of prior information in genetic association studies. When this prior information consists of estimates from association analyses of single-nucleotide polymorphisms (SNP)-intermediate or SNP-gene expression, a hierarchical model is equivalent to a 2-stage instrumental or transcriptome-wide association study (TWAS) analysis, respectively. We propose to extend our previous approach for the joint analysis of marginal summary statistics to incorporate prior information via a hierarchical model (hJAM). In this framework, the use of appropriate estimates as prior information yields an analysis similar to Mendelian randomization (MR) and TWAS approaches. hJAM is applicable to multiple correlated SNPs and intermediates to yield conditional estimates for the intermediates on the outcome, thus providing advantages over alternative approaches. We investigated the performance of hJAM in comparison with existing MR and TWAS approaches and demonstrated that hJAM yields an unbiased estimate, maintains correct type-I error, and has increased power across extensive simulations. We applied hJAM to 2 examples: estimating the causal effects of body mass index (GIANT Consortium) and type 2 diabetes (DIAGRAM data set, GERA Cohort, and UK Biobank) on myocardial infarction (UK Biobank) and estimating the causal effects of the expressions of the genes for nuclear casein kinase and cyclin dependent kinase substrate 1 and peptidase M20 domain containing 1 on the risk of prostate cancer (PRACTICAL and GTEx).

摘要

先前的研究已经证明了分层建模在将灵活的多种先验信息纳入遗传关联研究中的有用性。当这种先验信息由单核苷酸多态性(SNP)-中间物或 SNP-基因表达关联分析的估计值组成时,分层模型分别相当于两阶段工具或全转录组关联研究(TWAS)分析。我们建议扩展我们之前用于联合分析边缘汇总统计数据的方法,通过分层模型(hJAM)纳入先验信息。在这个框架中,使用适当的估计值作为先验信息会产生类似于孟德尔随机化(MR)和 TWAS 方法的分析。hJAM 适用于多个相关的 SNP 和中间物,以产生中间物对结局的条件估计,从而提供优于替代方法的优势。我们研究了 hJAM 与现有的 MR 和 TWAS 方法相比的性能,并证明 hJAM 产生了无偏估计,保持了正确的 I 型错误率,并在广泛的模拟中提高了功效。我们将 hJAM 应用于 2 个示例:估计体重指数(GIANT 联盟)和 2 型糖尿病(DIAGRAM 数据集、GERA 队列和英国生物库)对心肌梗死(英国生物库)的因果效应,以及估计核酪蛋白激酶和细胞周期依赖性激酶底物 1 和肽酶 M20 结构域包含 1 的基因表达对前列腺癌风险的因果效应(PRACTICAL 和 GTEx)。