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本文引用的文献

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An efficient weighted tag SNP-set analytical method in genome-wide association studies.全基因组关联研究中的一种高效加权标签单核苷酸多态性集分析方法。
BMC Genet. 2015 Mar 13;16:25. doi: 10.1186/s12863-015-0182-3.
2
Effect of a single nucleotide polymorphism in miR-146a on COX-2 protein expression and lung function in smokers with chronic obstructive pulmonary disease.miR-146a单核苷酸多态性对慢性阻塞性肺疾病吸烟者COX-2蛋白表达及肺功能的影响
Int J Chron Obstruct Pulmon Dis. 2015 Mar 4;10:463-73. doi: 10.2147/COPD.S74345. eCollection 2015.
3
Functional annotation of colon cancer risk SNPs.结肠癌风险单核苷酸多态性的功能注释。
Nat Commun. 2014 Sep 30;5:5114. doi: 10.1038/ncomms6114.
4
Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.CXCR2及其他基因中的罕见和低频编码变异与血液学特征相关。
Nat Genet. 2014 Jun;46(6):629-34. doi: 10.1038/ng.2962. Epub 2014 Apr 28.
5
Beyond GWASs: illuminating the dark road from association to function.超越 GWASs:从关联到功能照亮黑暗之路。
Am J Hum Genet. 2013 Nov 7;93(5):779-97. doi: 10.1016/j.ajhg.2013.10.012.
6
Kernel machine SNP-set testing under multiple candidate kernels.基于多个候选核的核机器 SNP 集检验。
Genet Epidemiol. 2013 Apr;37(3):267-75. doi: 10.1002/gepi.21715. Epub 2013 Mar 7.
7
Family-based association tests for sequence data, and comparisons with population-based association tests.基于家系的序列数据关联分析与基于群体的关联分析比较。
Eur J Hum Genet. 2013 Oct;21(10):1158-62. doi: 10.1038/ejhg.2012.308. Epub 2013 Feb 6.
8
Predicting functional effect of human missense mutations using PolyPhen-2.使用PolyPhen-2预测人类错义突变的功能效应。
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Kernel machine SNP-set analysis for censored survival outcomes in genome-wide association studies.基于核机器的全基因组关联研究中截尾生存结局的 SNP 集分析。
Genet Epidemiol. 2011 Nov;35(7):620-31. doi: 10.1002/gepi.20610. Epub 2011 Aug 4.
10
Rare-variant association testing for sequencing data with the sequence kernel association test.基于序列核关联检验的测序数据罕见变异关联分析
Am J Hum Genet. 2011 Jul 15;89(1):82-93. doi: 10.1016/j.ajhg.2011.05.029. Epub 2011 Jul 7.

在使用变量选择的核机器测试后对个体遗传变异进行优先级排序。

Prioritizing individual genetic variants after kernel machine testing using variable selection.

作者信息

He Qianchuan, Cai Tianxi, Liu Yang, Zhao Ni, Harmon Quaker E, Almli Lynn M, Binder Elisabeth B, Engel Stephanie M, Ressler Kerry J, Conneely Karen N, Lin Xihong, Wu Michael C

机构信息

Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.

Department of Biostatistics, Harvard School of Public Health, Boston, Massachusetts, United States of America.

出版信息

Genet Epidemiol. 2016 Dec;40(8):722-731. doi: 10.1002/gepi.21993. Epub 2016 Aug 3.

DOI:10.1002/gepi.21993
PMID:27488097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5118060/
Abstract

Kernel machine learning methods, such as the SNP-set kernel association test (SKAT), have been widely used to test associations between traits and genetic polymorphisms. In contrast to traditional single-SNP analysis methods, these methods are designed to examine the joint effect of a set of related SNPs (such as a group of SNPs within a gene or a pathway) and are able to identify sets of SNPs that are associated with the trait of interest. However, as with many multi-SNP testing approaches, kernel machine testing can draw conclusion only at the SNP-set level, and does not directly inform on which one(s) of the identified SNP set is actually driving the associations. A recently proposed procedure, KerNel Iterative Feature Extraction (KNIFE), provides a general framework for incorporating variable selection into kernel machine methods. In this article, we focus on quantitative traits and relatively common SNPs, and adapt the KNIFE procedure to genetic association studies and propose an approach to identify driver SNPs after the application of SKAT to gene set analysis. Our approach accommodates several kernels that are widely used in SNP analysis, such as the linear kernel and the Identity by State (IBS) kernel. The proposed approach provides practically useful utilities to prioritize SNPs, and fills the gap between SNP set analysis and biological functional studies. Both simulation studies and real data application are used to demonstrate the proposed approach.

摘要

核机器学习方法,如单核苷酸多态性集核关联检验(SKAT),已被广泛用于检验性状与基因多态性之间的关联。与传统的单核苷酸多态性分析方法不同,这些方法旨在检验一组相关单核苷酸多态性(如基因或通路内的一组单核苷酸多态性)的联合效应,并且能够识别与感兴趣的性状相关的单核苷酸多态性集合。然而,与许多多单核苷酸多态性检验方法一样,核机器检验只能在单核苷酸多态性集水平上得出结论,而不能直接告知所识别的单核苷酸多态性集中哪些实际上驱动了这种关联。最近提出的一种方法,核迭代特征提取(KNIFE),提供了一个将变量选择纳入核机器方法的通用框架。在本文中,我们关注数量性状和相对常见的单核苷酸多态性,并将KNIFE方法应用于基因关联研究,提出了一种在将SKAT应用于基因集分析后识别驱动单核苷酸多态性的方法。我们的方法适用于单核苷酸多态性分析中广泛使用的几种核,如线性核和状态一致性(IBS)核。所提出的方法为单核苷酸多态性的优先级排序提供了实际有用的工具,并填补了单核苷酸多态性集分析与生物学功能研究之间的空白。模拟研究和实际数据应用都被用来证明所提出的方法。