Marchani Elizabeth E, Wijsman Ellen M
Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195, USA.
Hum Hered. 2011;72(4):289-97. doi: 10.1159/000334083. Epub 2011 Dec 23.
Linkage analysis identifies markers that appear to be co-inherited with a trait within pedigrees. The inheritance of a chromosomal segment may be probabilistically reconstructed, with missing data complicating inference. Inheritance patterns are further obscured in the analysis of complex traits, where variants in one or more genes may contribute to phenotypic variation within a pedigree. In this case, determining which relatives share a trait variant is not simple. We describe how to represent these patterns of inheritance for marker loci. We summarize how to sample patterns of inheritance consistent with genotypic and pedigree data using gl_auto, available in MORGAN v3.0. We describe identification of classes of equivalent inheritance patterns with the program IBDgraph. We finally provide an example of how these programs may be used to simplify interpretation of linkage analysis of complex traits in general pedigrees. We borrow information across loci in a parametric linkage analysis of a large pedigree. We explore the contribution of each equivalence class to a linkage signal, illustrate estimated patterns of identity-by-descent sharing, and identify a haplotype tagging the chromosomal segment driving the linkage signal. Haplotype carriers are more likely to share the linked trait variant, and can be prioritized for subsequent DNA sequencing.
连锁分析可识别在系谱中似乎与某一性状共同遗传的标记。染色体片段的遗传情况可通过概率方法重建,但缺失数据会使推断变得复杂。在复杂性状分析中,遗传模式会进一步模糊,因为一个或多个基因中的变异可能导致系谱内的表型变异。在这种情况下,确定哪些亲属共享性状变异并非易事。我们描述了如何表示标记位点的这些遗传模式。我们总结了如何使用MORGAN v3.0中可用的gl_auto对与基因型和系谱数据一致的遗传模式进行采样。我们描述了使用程序IBDgraph识别等效遗传模式类别的方法。我们最后给出一个示例,说明如何使用这些程序来简化一般系谱中复杂性状连锁分析的解释。在对一个大型系谱进行参数连锁分析时,我们跨位点借用信息。我们探讨每个等效类对连锁信号的贡献,说明估计的同源等位基因共享模式,并识别标记驱动连锁信号的染色体片段的单倍型。单倍型携带者更有可能共享连锁的性状变异,可将其作为后续DNA测序的优先对象。