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本文引用的文献

1
Detecting rare haplotype-environment interaction with logistic Bayesian LASSO.利用逻辑贝叶斯 LASSO 检测罕见单倍型-环境交互作用。
Genet Epidemiol. 2014 Jan;38(1):31-41. doi: 10.1002/gepi.21773. Epub 2013 Nov 23.
2
Logistic Bayesian LASSO for identifying association with rare haplotypes and application to age-related macular degeneration.用于识别与罕见单倍型关联的逻辑贝叶斯套索法及其在年龄相关性黄斑变性中的应用。
Biometrics. 2012 Jun;68(2):587-97. doi: 10.1111/j.1541-0420.2011.01680.x. Epub 2011 Sep 28.
3
Gene--environment-wide association studies: emerging approaches.基因-环境全基因组关联研究:新兴方法。
Nat Rev Genet. 2010 Apr;11(4):259-72. doi: 10.1038/nrg2764.
4
Genetic polymorphisms of MPO, GSTT1, GSTM1, GSTP1, EPHX1 and NQO1 as risk factors of early-onset lung cancer.MPO、GSTT1、GSTM1、GSTP1、EPHX1 和 NQO1 基因多态性与早发性肺癌的风险因素。
Int J Cancer. 2010 Oct 1;127(7):1547-61. doi: 10.1002/ijc.25175.
5
Finding the missing heritability of complex diseases.寻找复杂疾病中缺失的遗传力。
Nature. 2009 Oct 8;461(7265):747-53. doi: 10.1038/nature08494.
6
Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression.I期代谢基因与肺癌风险:多种多态性及mRNA表达
PLoS One. 2009 May 21;4(5):e5652. doi: 10.1371/journal.pone.0005652.
7
Genomewide association studies--illuminating biologic pathways.全基因组关联研究——揭示生物学通路
N Engl J Med. 2009 Apr 23;360(17):1699-701. doi: 10.1056/NEJMp0808934. Epub 2009 Apr 15.
8
Common genetic variation and human traits.常见基因变异与人类性状
N Engl J Med. 2009 Apr 23;360(17):1696-8. doi: 10.1056/NEJMp0806284. Epub 2009 Apr 15.
9
Genetic risk prediction--are we there yet?基因风险预测——我们做到了吗?
N Engl J Med. 2009 Apr 23;360(17):1701-3. doi: 10.1056/NEJMp0810107. Epub 2009 Apr 15.
10
Personal genomes: The case of the missing heritability.个人基因组:“缺失的遗传力”问题
Nature. 2008 Nov 6;456(7218):18-21. doi: 10.1038/456018a.

用于检测罕见单倍型与环境相互作用并应用于肺癌的逻辑贝叶斯LASSO改进版本。

An Improved Version of Logistic Bayesian LASSO for Detecting Rare Haplotype-Environment Interactions with Application to Lung Cancer.

作者信息

Zhang Yuan, Biswas Swati

机构信息

Department of Mathematical Sciences, University of Texas at Dallas, Richardson, TX, USA.

出版信息

Cancer Inform. 2015 Feb 9;14(Suppl 2):11-6. doi: 10.4137/CIN.S17290. eCollection 2015.

DOI:10.4137/CIN.S17290
PMID:25733797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4332044/
Abstract

The importance of haplotype association and gene-environment interactions (GxE) in the context of rare variants has been underlined in voluminous literature. Recently, a software based on logistic Bayesian LASSO (LBL) was proposed for detecting GxE, where G is a rare (or common) haplotype variant (rHTV)-it is called LBL-GxE. However, it required relatively long computation time and could handle only one environmental covariate with two levels. Here we propose an improved version of LBL-GxE, which is not only computationally faster but can also handle multiple covariates, each with multiple levels. We also discuss details of the software, including input, output, and some options. We apply LBL-GxE to a lung cancer dataset and find a rare haplotype with protective effect for current smokers. Our results indicate that LBL-GxE, especially with the improvements proposed here, is a useful and computationally viable tool for investigating rare haplotype interactions.

摘要

在大量文献中,单倍型关联以及基因-环境相互作用(GxE)在罕见变异背景下的重要性已得到强调。最近,有人提出了一种基于逻辑贝叶斯套索(LBL)的软件来检测GxE,其中G是一种罕见(或常见)的单倍型变异(rHTV)——它被称为LBL-GxE。然而,它需要相对较长的计算时间,并且只能处理具有两个水平的一个环境协变量。在此,我们提出了LBL-GxE的一个改进版本,它不仅计算速度更快,而且还能处理多个协变量,每个协变量都有多个水平。我们还讨论了该软件的细节,包括输入、输出和一些选项。我们将LBL-GxE应用于一个肺癌数据集,并发现一种对当前吸烟者具有保护作用的罕见单倍型。我们的结果表明,LBL-GxE,尤其是结合此处提出的改进,是研究罕见单倍型相互作用的一个有用且在计算上可行的工具。