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基于定量性状和 Mantel 统计量的酒精依赖单体型共享分析。

Haplotype-sharing analysis for alcohol dependence based on quantitative traits and the Mantel statistic.

机构信息

Institute of Medical Biometry and Statistics, University Hospital Schleswig-Holstein, Campus Lübeck, University at Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.

出版信息

BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S75. doi: 10.1186/1471-2156-6-S1-S75.

DOI:10.1186/1471-2156-6-S1-S75
PMID:16451689
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1866706/
Abstract

Haplotype-based methods have become increasingly popular in the last decade because shared lengths in haplotypes can be used for disease localization. In this contribution, we propose a novel linkage-based haplotype-sharing approach for quantitative traits based on the class of Mantel statistics which is closely related to the weighted pair-wise correlation statistic. Because these statistics are known to be liberal, we propose a permutation test to evaluate significance. We applied the Mantel statistic to the autosomal data from the genome-wide scan of the Collaborative Study on the Genetics of Alcoholism with the Affymetrix Genotype 10 K array that was provided for the Genetic Analysis Workshop 14. Four regions on chromosome 4, 8, 16, and 20 showed p-values less than 0.005 with a minimum p-value of < 0.0001 on chromosome 16 (tsc0520638 at 72.8 cM). Three of these four regions located on chromosome 4, 16, and 20 have been reported previously in the Genetic Analysis Workshop 11.

摘要

基于单体型的方法在过去十年中变得越来越流行,因为单体型中的共享长度可用于疾病定位。在本研究中,我们提出了一种基于连锁的新型单体型共享方法,用于基于 Mantel 统计量的数量性状,该统计量与加权成对相关统计量密切相关。由于这些统计量被认为是宽松的,我们提出了一种置换检验来评估其显著性。我们将 Mantel 统计量应用于合作酒精中毒遗传学基因组扫描的常染色体数据,该数据由 Affymetrix Genotype 10 K 阵列提供,用于 14 届遗传分析研讨会。在染色体 4、8、16 和 20 上有四个区域的 p 值小于 0.005,在染色体 16 上的最小 p 值小于 0.0001(72.8 cM 处的 tsc0520638)。这四个区域中的三个位于染色体 4、16 和 20 上,之前在 11 届遗传分析研讨会上有报道过。

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本文引用的文献

1
Exploring haplotype sharing methods in general and isolated populations to detect gene(s) of a complex genetic trait.探索一般人群和隔离人群中的单倍型共享方法,以检测复杂遗传性状的基因。
Genet Epidemiol. 2001;21 Suppl 1:S554-9. doi: 10.1002/gepi.2001.21.s1.s554.
2
Genome search for alcohol dependence using the weighted pairwise correlation linkage method: interesting findings on chromosome 4.使用加权成对相关连锁法对酒精依赖进行全基因组搜索:4号染色体上的有趣发现。
Genet Epidemiol. 1999;17 Suppl 1:S421-6. doi: 10.1002/gepi.1370170771.
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Genome-wide linkage analysis using genetic variance components of alcohol dependency-associated censored and continuous traits.
Genet Epidemiol. 1999;17 Suppl 1:S283-8. doi: 10.1002/gepi.1370170748.
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Alcoholism as a complex trait: comparison of genetic models and role of epidemiological risk factors.
Genet Epidemiol. 1999;17 Suppl 1:S247-52. doi: 10.1002/gepi.1370170742.
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Exploring the impact of extended phenotype in stratified samples.
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Monte Carlo Markov chain methods for genome screening.用于基因组筛选的蒙特卡罗马尔可夫链方法。
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Genomic sharing surrounding alleles identical by descent: effects of genetic drift and population growth.同源等位基因周围的基因组共享:遗传漂变和种群增长的影响
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Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspring.对至少有一个患病后代的核心家庭中患病个体进行单倍型共享分析。
Genet Epidemiol. 1997;14(6):915-20. doi: 10.1002/(SICI)1098-2272(1997)14:6<915::AID-GEPI59>3.0.CO;2-P.
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Improving the robustness of the weighted pairwise correlation test for linkage analysis.提高用于连锁分析的加权成对相关性检验的稳健性。
Genet Epidemiol. 1996;13(6):559-73. doi: 10.1002/(SICI)1098-2272(1996)13:6<559::AID-GEPI3>3.0.CO;2-W.