• 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

从 GWAS 错误中学习:从实验设计到科学方法。

Learning from our GWAS mistakes: from experimental design to scientific method.

机构信息

Golden Helix Inc., Bozeman, MT 59719, USA.

出版信息

Biostatistics. 2012 Apr;13(2):195-203. doi: 10.1093/biostatistics/kxr055. Epub 2012 Jan 27.

DOI:10.1093/biostatistics/kxr055
PMID:22285994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3297828/
Abstract

Many public and private genome-wide association studies that we have analyzed include flaws in design, with avoidable confounding appearing as a norm rather than the exception. Rather than recognizing flawed research design and addressing that, a category of quality-control statistical methods has arisen to treat only the symptoms. Reflecting more deeply, we examine elements of current genomic research in light of the traditional scientific method and find that hypotheses are often detached from data collection, experimental design, and causal theories. Association studies independent of causal theories, along with multiple testing errors, too often drive health care and public policy decisions. In an era of large-scale biological research, we ask questions about the role of statistical analyses in advancing coherent theories of diseases and their mechanisms. We advocate for reinterpretation of the scientific method in the context of large-scale data analysis opportunities and for renewed appreciation of falsifiable hypotheses, so that we can learn more from our best mistakes.

摘要

我们分析过的许多公共和私人全基因组关联研究都存在设计缺陷,可避免的混杂现象似乎是常态而非例外。人们没有认识到有缺陷的研究设计并加以解决,而是出现了一类质量控制统计方法,这些方法只是针对症状进行处理。我们进一步深入思考,根据传统的科学方法来审视当前基因组研究的各个要素,结果发现假设往往与数据收集、实验设计和因果理论脱节。与因果理论无关的关联研究以及多次测试错误,往往会左右医疗保健和公共政策决策。在大规模生物研究时代,我们对统计分析在推进疾病及其机制的连贯理论方面所起的作用提出了质疑。我们提倡在大规模数据分析机会的背景下重新解释科学方法,并重新重视可证伪的假设,以便我们能够从最好的错误中吸取更多的教训。

相似文献

1
Learning from our GWAS mistakes: from experimental design to scientific method.从 GWAS 错误中学习:从实验设计到科学方法。
Biostatistics. 2012 Apr;13(2):195-203. doi: 10.1093/biostatistics/kxr055. Epub 2012 Jan 27.
2
Bayesian multivariate reanalysis of large genetic studies identifies many new associations.贝叶斯多变量重新分析大型遗传研究确定了许多新的关联。
PLoS Genet. 2019 Oct 9;15(10):e1008431. doi: 10.1371/journal.pgen.1008431. eCollection 2019 Oct.
3
Genome-wide association data classification and SNPs selection using two-stage quality-based Random Forests.使用基于质量的两阶段随机森林进行全基因组关联数据分类和单核苷酸多态性选择。
BMC Genomics. 2015;16 Suppl 2(Suppl 2):S5. doi: 10.1186/1471-2164-16-S2-S5. Epub 2015 Jan 21.
4
repfdr: a tool for replicability analysis for genome-wide association studies.repfdr:用于全基因组关联研究复制分析的工具。
Bioinformatics. 2014 Oct 15;30(20):2971-2. doi: 10.1093/bioinformatics/btu434. Epub 2014 Jul 9.
5
Detecting associated single-nucleotide polymorphisms on the X chromosome in case control genome-wide association studies.在病例对照全基因组关联研究中检测X染色体上的相关单核苷酸多态性。
Stat Methods Med Res. 2017 Apr;26(2):567-582. doi: 10.1177/0962280214551815. Epub 2014 Sep 24.
6
GW-SEM: A Statistical Package to Conduct Genome-Wide Structural Equation Modeling.GW-SEM:一个用于进行全基因组结构方程建模的统计软件包。
Behav Genet. 2017 May;47(3):345-359. doi: 10.1007/s10519-017-9842-6. Epub 2017 Mar 15.
7
Statistical selection of biological models for genome-wide association analyses.全基因组关联分析中生物模型的统计选择。
Methods. 2018 Aug 1;145:67-75. doi: 10.1016/j.ymeth.2018.05.019. Epub 2018 May 25.
8
Powerful statistical method to detect disease-associated genes using publicly available genome-wide association studies summary data.利用公开的全基因组关联研究汇总数据,使用强大的统计方法来检测疾病相关基因。
Genet Epidemiol. 2019 Dec;43(8):941-951. doi: 10.1002/gepi.22251. Epub 2019 Aug 7.
9
The future of Cochrane Neonatal.考克兰新生儿协作网的未来。
Early Hum Dev. 2020 Nov;150:105191. doi: 10.1016/j.earlhumdev.2020.105191. Epub 2020 Sep 12.
10
Statistical perspectives for genome-wide association studies (GWAS).全基因组关联研究(GWAS)的统计学视角
Methods Mol Biol. 2014;1168:47-61. doi: 10.1007/978-1-4939-0847-9_4.

引用本文的文献

1
Learning Lessons on Reproducibility and Replicability in Large Scale Genome-Wide Association Studies.从大规模全基因组关联研究中的可重复性和可复制性中吸取经验教训。
Harv Data Sci Rev. 2020 Fall;2(4). doi: 10.1162/99608f92.33703976. Epub 2020 Dec 16.
2
Open Science Practices in Psychiatric Genetics: A Primer.精神遗传学中的开放科学实践:入门指南。
Biol Psychiatry Glob Open Sci. 2023 Aug 22;4(1):110-119. doi: 10.1016/j.bpsgos.2023.08.007. eCollection 2024 Jan.
3
Genome-Environment Associations, an Innovative Tool for Studying Heritable Evolutionary Adaptation in Orphan Crops and Wild Relatives.基因组-环境关联分析:研究孤儿作物及其野生近缘种可遗传进化适应的创新工具
Front Genet. 2022 Aug 5;13:910386. doi: 10.3389/fgene.2022.910386. eCollection 2022.
4
TIGA: target illumination GWAS analytics.TIGA:目标照明全基因组关联分析。
Bioinformatics. 2021 Nov 5;37(21):3865-3873. doi: 10.1093/bioinformatics/btab427.
5
Harnessing Crop Wild Diversity for Climate Change Adaptation.利用作物野生多样性适应气候变化。
Genes (Basel). 2021 May 20;12(5):783. doi: 10.3390/genes12050783.
6
Omixer: multivariate and reproducible sample randomization to proactively counter batch effects in omics studies.Omixer:多元且可重复的样本随机化,可主动应对组学研究中的批次效应。
Bioinformatics. 2021 Sep 29;37(18):3051-3052. doi: 10.1093/bioinformatics/btab159.
7
Predicting Thermal Adaptation by Looking Into Populations' Genomic Past.通过探究群体的基因组历史来预测热适应性。
Front Genet. 2020 Sep 25;11:564515. doi: 10.3389/fgene.2020.564515. eCollection 2020.
8
Novel Bead-Based Epitope Assay is a sensitive and reliable tool for profiling epitope-specific antibody repertoire in food allergy.新型珠基表位分析是一种用于分析食物过敏中表位特异性抗体库的敏感可靠的工具。
Sci Rep. 2019 Dec 5;9(1):18425. doi: 10.1038/s41598-019-54868-7.
9
Perspective: Dimensions of the scientific method.观点:科学方法的维度。
PLoS Comput Biol. 2019 Sep 12;15(9):e1007279. doi: 10.1371/journal.pcbi.1007279. eCollection 2019 Sep.
10
Harnessing Human Microphysiology Systems as Key Experimental Models for Quantitative Systems Pharmacology.利用人体微生理学系统作为定量系统药理学的关键实验模型。
Handb Exp Pharmacol. 2019;260:327-367. doi: 10.1007/164_2019_239.

本文引用的文献

1
Retraction.撤回。
Science. 2011 Jul 22;333(6041):404. doi: 10.1126/science.333.6041.404-a.
2
Editorial expression of concern.编辑关注声明。
Science. 2010 Nov 12;330(6006):912. doi: 10.1126/science.330.6006.912-b.
3
Tackling the widespread and critical impact of batch effects in high-throughput data.解决高通量数据中广泛存在且极具影响力的批次效应问题。
Nat Rev Genet. 2010 Oct;11(10):733-9. doi: 10.1038/nrg2825. Epub 2010 Sep 14.
4
Genetic signatures of exceptional longevity in humans.人类超长寿命的遗传特征。
Science. 2010 Jul 1;2010. doi: 10.1126/science.1190532.
5
Why current publication practices may distort science.为何当前的出版行为可能会扭曲科学。
PLoS Med. 2008 Oct 7;5(10):e201. doi: 10.1371/journal.pmed.0050201.
6
Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.流行病学观察性研究报告强化(STROBE)声明:观察性研究报告指南
BMJ. 2007 Oct 20;335(7624):806-8. doi: 10.1136/bmj.39335.541782.AD.
7
THE METHOD OF MULTIPLE WORKING HYPOTHESES.多重工作假设法
Science. 1890 Feb 7;15(366):92-6. doi: 10.1126/science.ns-15.366.92.
8
Strong Inference: Certain systematic methods of scientific thinking may produce much more rapid progress than others.强推理:某些系统的科学思维方法可能比其他方法产生更快的进展。
Science. 1964 Oct 16;146(3642):347-53. doi: 10.1126/science.146.3642.347.
9
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.对14000例七种常见疾病患者及3000例共享对照进行全基因组关联研究。
Nature. 2007 Jun 7;447(7145):661-78. doi: 10.1038/nature05911.
10
Why most published research findings are false.为何大多数已发表的研究结果是错误的。
PLoS Med. 2005 Aug;2(8):e124. doi: 10.1371/journal.pmed.0020124. Epub 2005 Aug 30.