Suppr超能文献

在候选基因研究中合并三联体和无关个体的数据:在睾丸癌数据中的应用

On combining triads and unrelated subjects data in candidate gene studies: an application to data on testicular cancer.

作者信息

Hsu Li, Starr Jacqueline R, Zheng Yingye, Schwartz Stephen M

机构信息

Biostatistics and Biomathematics Program, Fred Hutchinson Cancer Research Center, Seattle, Wash., USA.

出版信息

Hum Hered. 2009;67(2):88-103. doi: 10.1159/000179557. Epub 2008 Dec 12.

Abstract

Combining data collected from different sources is a cost-effective and time-efficient approach for enhancing the statistical efficiency in estimating weak-to-modest genetic effects or gene-gene or gene-environment interactions. However, combining data across studies becomes complicated when data are collected under different study designs, such as family-based and unrelated individual-based (e.g., population-based case-control design). In this paper, we describe a general method that permits the joint estimation of effects on disease risk of genes, environmental factors, and gene-gene/gene-environment interactions under a hybrid design that includes cases, parents of cases, and unrelated individuals. We provide both asymptotic theory and statistical inference. Extensive simulation experiments demonstrate that the proposed estimation and inferential methods perform well in realistic settings. We illustrate the method by an application to a study of testicular cancer.

摘要

整合从不同来源收集的数据是一种经济高效且节省时间的方法,可提高在估计微弱至中等程度的遗传效应或基因-基因或基因-环境相互作用时的统计效率。然而,当数据是在不同的研究设计下收集时,跨研究整合数据就变得复杂了,例如基于家系的设计和基于非亲属个体的设计(如基于人群的病例对照设计)。在本文中,我们描述了一种通用方法,该方法允许在包含病例、病例的父母以及非亲属个体的混合设计下,联合估计基因、环境因素以及基因-基因/基因-环境相互作用对疾病风险的影响。我们提供了渐近理论和统计推断。大量的模拟实验表明,所提出的估计和推断方法在实际情况下表现良好。我们通过应用于睾丸癌研究来说明该方法。

相似文献

2
On combining family-based and population-based case-control data in association studies.
Biometrics. 2010 Dec;66(4):1024-33. doi: 10.1111/j.1541-0420.2010.01393.x.
3
Genetic association analysis using data from triads and unrelated subjects.
Am J Hum Genet. 2005 Apr;76(4):592-608. doi: 10.1086/429225. Epub 2005 Feb 14.
4
Predisposition alleles for Testicular Germ Cell Tumour.
Curr Opin Genet Dev. 2010 Jun;20(3):225-30. doi: 10.1016/j.gde.2010.02.006. Epub 2010 Mar 19.
5
A hybrid design: case-parent triads supplemented by control-mother dyads.
Genet Epidemiol. 2009 Feb;33(2):136-44. doi: 10.1002/gepi.20365.
6
Simulating autosomal genotypes with realistic linkage disequilibrium and a spiked-in genetic effect.
BMC Bioinformatics. 2018 Jan 2;19(1):2. doi: 10.1186/s12859-017-2004-2.
9
Genetic variation in AKT1, PTEN and the 8q24 locus, and the risk of testicular germ cell tumor.
Hum Reprod. 2013 Jul;28(7):1995-2002. doi: 10.1093/humrep/det127. Epub 2013 May 2.

本文引用的文献

1
PedGenie: meta genetic association testing in mixed family and case-control designs.
BMC Bioinformatics. 2007 Nov 15;8:448. doi: 10.1186/1471-2105-8-448.
2
Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer.
Cancer Epidemiol Biomarkers Prev. 2007 Nov;16(11):2331-43. doi: 10.1158/1055-9965.EPI-07-0648. Epub 2007 Nov 2.
3
Genetic and environmental risk factors for testicular cancer.
Int J Androl. 2007 Aug;30(4):230-40; discussion 240-1. doi: 10.1111/j.1365-2605.2007.00760.x.
4
Dealing with missing data in family-based association studies: a multiple imputation approach.
Hum Hered. 2007;63(3-4):229-38. doi: 10.1159/000100481. Epub 2007 Mar 7.
7
Family-based designs in the age of large-scale gene-association studies.
Nat Rev Genet. 2006 May;7(5):385-94. doi: 10.1038/nrg1839.
9
Population-based family studies in genetic epidemiology.
Lancet. 2005;366(9494):1397-406. doi: 10.1016/S0140-6736(05)67570-8.
10
A hybrid design for studying genetic influences on risk of diseases with onset early in life.
Am J Hum Genet. 2005 Oct;77(4):627-36. doi: 10.1086/496900. Epub 2005 Aug 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验