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Comparing single-nucleotide polymorphism marker-based and microsatellite marker-based linkage analyses

机译:比较基于单核苷酸多态性标记和基于微卫星标记的连锁分析

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摘要

We compared linkage analysis results for an alcoholism trait, ALDX1 (DSM-III-R and Feigner criteria) using a nonparametric linkage analysis method, which takes into account allele sharing among several affected persons, for both microsatellite and single-nucleotide polymorphism (SNP) markers (Affymetrix and Illumina) in the Collaborative Study on the Genetics of Alcoholism (COGA) dataset provided to participants at the Genetic Analysis Workshop 14 (GAW14). The two sets of linkage results from the dense Affymetrix SNP markers and less densely spaced Illumina SNP markers are very similar. The linkage analysis results from microsatellite and SNP markers are generally similar, but the match is not perfect. Strong linkage peaks were found on chromosome 7 in three sets of linkage analyses using both SNP and microsatellite marker data. We also observed that for SNP markers, using the given genetic map and using the map by converting 1 megabase pair (1 Mb) to 1 centimorgan (cM), did not change the linkage results. We recommend the use of the 1 Mb-to-1 cM converted map in a first round of linkage analysis with SNP markers in which map integration is an issue.
机译:我们使用非参数连锁分析方法比较了酒精中毒特征ALDX1(DSM-III-R和Feigner标准)的连锁分析结果,该方法考虑了多个受影响人之间的等位基因共享,包括微卫星和单核苷酸多态性(SNP)酒精中毒遗传学(COGA)数据集的合作研究中的标记(Affymetrix和Illumina)提供给了遗传分析研讨会14(GAW14)的参与者。密集Affymetrix SNP标记与低密度Illumina SNP标记的两组连接非常相似。来自微卫星和SNP标记的连锁分析结果通常相似,但是匹配并不完美。在使用SNP和微卫星标记数据进行的三组连锁分析中,在7号染色体上发现了强连锁峰。我们还观察到,对于SNP标记,使用给定的遗传图谱以及通过将1兆碱基对(1 Mb)转换为1 centimorgan(cM)来使用该图谱不会改变连锁结果。我们建议在第一轮与SNP标记的连锁分析中使用从1 Mb到1 cM转换的图,其中图整合是一个问题。

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