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本文引用的文献

1
An imputed genotype resource for the laboratory mouse.实验室小鼠的推断基因型资源。
Mamm Genome. 2008 Mar;19(3):199-208. doi: 10.1007/s00335-008-9098-9. Epub 2008 Feb 27.
2
On the subspecific origin of the laboratory mouse.论实验小鼠的亚种起源。
Nat Genet. 2007 Sep;39(9):1100-7. doi: 10.1038/ng2087. Epub 2007 Jul 29.
3
TreeDT: tree pattern mining for gene mapping.TreeDT:用于基因图谱绘制的树模式挖掘
IEEE/ACM Trans Comput Biol Bioinform. 2006 Apr-Jun;3(2):174-85. doi: 10.1109/TCBB.2006.28.
4
Whole genome association mapping by incompatibilities and local perfect phylogenies.基于不相容性和局部完美系统发育的全基因组关联图谱绘制。
BMC Bioinformatics. 2006 Oct 16;7:454. doi: 10.1186/1471-2105-7-454.
5
Mapping trait loci by use of inferred ancestral recombination graphs.利用推断的祖先重组图定位性状基因座。
Am J Hum Genet. 2006 Nov;79(5):910-22. doi: 10.1086/508901. Epub 2006 Sep 27.
6
Evaluating and improving power in whole-genome association studies using fixed marker sets.使用固定标记集评估和提高全基因组关联研究的效能
Nat Genet. 2006 Jun;38(6):663-7. doi: 10.1038/ng1816. Epub 2006 May 21.
7
Comparative analysis of haplotype association mapping algorithms.单倍型关联定位算法的比较分析
BMC Bioinformatics. 2006 Feb 9;7:61. doi: 10.1186/1471-2105-7-61.
8
Fine mapping of disease genes via haplotype clustering.通过单倍型聚类对疾病基因进行精细定位。
Genet Epidemiol. 2006 Feb;30(2):170-9. doi: 10.1002/gepi.20134.
9
Haplotype-based linkage disequilibrium mapping via direct data mining.通过直接数据挖掘进行基于单倍型的连锁不平衡图谱分析。
Bioinformatics. 2005 Dec 15;21(24):4384-93. doi: 10.1093/bioinformatics/bti732. Epub 2005 Oct 25.
10
CoaSim: a flexible environment for simulating genetic data under coalescent models.CoaSim:一种用于在溯祖模型下模拟遗传数据的灵活环境。
BMC Bioinformatics. 2005 Oct 14;6:252. doi: 10.1186/1471-2105-6-252.

TreeQA:使用局部完美系统发育树进行全基因组关联定量定位

TreeQA: quantitative genome wide association mapping using local perfect phylogeny trees.

作者信息

Pan Feng, McMillan Leonard, Pardo-Manuel De Villena Fernando, Threadgill David, Wang Wei

机构信息

Department of Computer Science, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Pac Symp Biocomput. 2009:415-26.

PMID:19209719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2739990/
Abstract

The goal of genome wide association (GWA) mapping in modern genetics is to identify genes or narrow regions in the genome that contribute to genetically complex phenotypes such as morphology or disease. Among the existing methods, tree-based association mapping methods show obvious advantages over single marker-based and haplotype-based methods because they incorporate information about the evolutionary history of the genome into the analysis. However, existing tree-based methods are designed primarily for binary phenotypes derived from case/control studies or fail to scale genome-wide. In this paper, we introduce TreeQA, a quantitative GWA mapping algorithm. TreeQA utilizes local perfect phylogenies constructed in genomic regions exhibiting no evidence of historical recombination. By efficient algorithm design and implementation, TreeQA can efficiently conduct quantitative genom-wide association analysis and is more effective than the previous methods. We conducted extensive experiments on both simulated datasets and mouse inbred lines to demonstrate the efficiency and effectiveness of TreeQA.

摘要

现代遗传学中全基因组关联(GWA)图谱绘制的目标是识别基因组中有助于形成形态或疾病等遗传复杂表型的基因或狭窄区域。在现有方法中,基于树的关联图谱绘制方法相对于基于单标记和基于单倍型的方法具有明显优势,因为它们将有关基因组进化历史的信息纳入了分析。然而,现有的基于树的方法主要是为病例/对照研究得出的二元表型设计的,或者无法进行全基因组规模的分析。在本文中,我们介绍了一种定量GWA图谱绘制算法TreeQA。TreeQA利用在没有历史重组证据的基因组区域构建的局部完美系统发育树。通过高效的算法设计与实现,TreeQA能够有效地进行全基因组定量关联分析,并且比以前的方法更有效。我们在模拟数据集和小鼠近交系上都进行了广泛的实验,以证明TreeQA的效率和有效性。