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通过统一连锁分析和关联分析提高定位精度。

Improvement of mapping accuracy by unifying linkage and association analysis.

作者信息

Lou Xiang-Yang, Ma Jennie Z, Yang Mark C K, Zhu Jun, Liu Peng-Yuan, Deng Hong-Wen, Elston Robert C, Li Ming D

机构信息

Department of Psychiatric Medicine, University of Virginia, Charlottesville, Virginia 22911, USA.

出版信息

Genetics. 2006 Jan;172(1):647-61. doi: 10.1534/genetics.105.045781. Epub 2005 Sep 19.

Abstract

It is well known that pedigree/family data record information on the coexistence in founder haplotypes of alleles at nearby loci and the cotransmission from parent to offspring that reveal different, but complementary, profiles of the genetic architecture. Either conventional linkage analysis that assumes linkage equilibrium or family-based association tests (FBATs) capture only partial information, leading to inefficiency. For example, FBATs will fail to detect even very tight linkage in the case where no allelic association exists, while a violation of the assumption of linkage equilibrium will result in biased estimation and reduced efficiency in linkage mapping. In this article, by using a data augmentation technique and the EM algorithm, we propose a likelihood-based approach that embeds both linkage and association analyses into a unified framework for general pedigree data. Relative to either linkage or association analysis, the proposed approach is expected to have greater estimation accuracy and power. Monte Carlo simulations support our theoretical expectations and demonstrate that our new methodology: (1) is more powerful than either FBATs or classic linkage analysis; (2) can unbiasedly estimate genetic parameters regardless of whether association exists, thus remedying the bias and less precision of traditional linkage analysis in the presence of association; and (3) is capable of identifying tight linkage alone. The new approach also holds the theoretical advantage that it can extract statistical information to the maximum extent and thereby improve mapping accuracy and power because it integrates multilocus population-based association study and pedigree-based linkage analysis into a coherent framework. Furthermore, our method is numerically stable and computationally efficient, as compared to existing parametric methods that use the simplex algorithm or Newton-type methods to maximize high-order multidimensional likelihood functions, and also offers the computation of Fisher's information matrix. Finally, we apply our methodology to a genetic study on bone mineral density (BMD) for the vitamin D receptor (VDR) gene and find that VDR is significantly linked to BMD at the one-third region of the wrist.

摘要

众所周知,系谱/家族数据记录了创始单倍型中附近位点等位基因的共存情况以及从亲代到子代的共传递情况,这些揭示了遗传结构的不同但互补的特征。无论是假设连锁平衡的传统连锁分析还是基于家族的关联检验(FBAT)都只捕捉到了部分信息,导致效率低下。例如,在不存在等位基因关联的情况下,FBAT甚至无法检测到非常紧密的连锁,而违反连锁平衡假设将导致连锁图谱估计有偏差且效率降低。在本文中,我们通过使用数据增强技术和期望最大化(EM)算法,提出了一种基于似然的方法,该方法将连锁分析和关联分析都嵌入到一个用于一般系谱数据的统一框架中。相对于连锁分析或关联分析,所提出的方法预计具有更高的估计准确性和检验效能。蒙特卡罗模拟支持了我们的理论预期,并证明了我们的新方法:(1)比FBAT或经典连锁分析更具检验效能;(2)无论是否存在关联,都能无偏地估计遗传参数,从而纠正了存在关联时传统连锁分析的偏差和较低的精度;(3)能够单独识别紧密连锁。新方法还具有理论优势,即它可以最大程度地提取统计信息,从而提高定位准确性和检验效能,因为它将基于多位点群体的关联研究和基于系谱的连锁分析整合到了一个连贯的框架中。此外,与现有的使用单纯形算法或牛顿型方法来最大化高阶多维似然函数的参数方法相比,我们的方法在数值上是稳定的且计算效率高,并且还提供了费舍尔信息矩阵的计算。最后,我们将我们的方法应用于维生素D受体(VDR)基因的骨矿物质密度(BMD)遗传研究,发现VDR在腕部三分之一区域与BMD显著连锁。

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本文引用的文献

1
Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal.
Am J Hum Genet. 2005 Jun;76(6):934-49. doi: 10.1086/430277. Epub 2005 Apr 5.
3
Whole-genome patterns of common DNA variation in three human populations.
Science. 2005 Feb 18;307(5712):1072-9. doi: 10.1126/science.1105436.
4
Association testing in a linked region using large pedigrees.
Am J Hum Genet. 2005 Mar;76(3):538-42. doi: 10.1086/428628. Epub 2005 Jan 18.
6
The International HapMap Project.
Nature. 2003 Dec 18;426(6968):789-96. doi: 10.1038/nature02168.
9
Power and design considerations for a general class of family-based association tests: quantitative traits.
Am J Hum Genet. 2002 Dec;71(6):1330-41. doi: 10.1086/344696. Epub 2002 Nov 21.
10
Power calculations for a general class of family-based association tests: dichotomous traits.
Am J Hum Genet. 2002 Sep;71(3):575-84. doi: 10.1086/342406. Epub 2002 Aug 12.

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