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Quantitative Trait Locus Mapping Methods for Diversity Outbred Mice

机译:多样性近交小鼠的数量性状基因座定位方法

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摘要

Genetic mapping studies in the mouse and other model organisms are used to search for genes underlying complex phenotypes. Traditional genetic mapping studies that employ single-generation crosses have poor mapping resolution and limit discovery to loci that are polymorphic between the two parental strains. Multiparent outbreeding populations address these shortcomings by increasing the density of recombination events and introducing allelic variants from multiple founder strains. However, multiparent crosses present new analytical challenges and require specialized software to take full advantage of these benefits. Each animal in an outbreeding population is genetically unique and must be genotyped using a high-density marker set; regression models for mapping must accommodate multiple founder alleles, and complex breeding designs give rise to polygenic covariance among related animals that must be accounted for in mapping analysis. The Diversity Outbred (DO) mice combine the genetic diversity of eight founder strains in a multigenerational breeding design that has been maintained for >16 generations. The large population size and randomized mating ensure the long-term genetic stability of this population. We present a complete analytical pipeline for genetic mapping in DO mice, including algorithms for probabilistic reconstruction of founder haplotypes from genotyping array intensity data, and mapping methods that accommodate multiple founder haplotypes and account for relatedness among animals. Power analysis suggests that studies with as few as 200 DO mice can detect loci with large effects, but loci that account for <5% of trait variance may require a sample size of up to 1000 animals. The methods described here are implemented in the freely available R package DOQTL.
机译:在小鼠和其他模型生物中的遗传图谱研究被用于寻找复杂表型的基因。采用单代杂交的传统遗传作图研究具有较差的作图分辨率,并将发现仅限于两个亲本菌株之间具有多态性的基因座。多亲近交群体通过增加重组事件的密度并引入多个始祖菌株的等位基因变体来解决这些缺点。然而,多亲杂交带来了新的分析挑战,需要专门的软件才能充分利用这些优势。远交种群中的每只动物在遗传上都是独特的,必须使用高密度标记集进行基因分型。用于作图的回归模型必须容纳多个创始人等位基因,复杂的育种设计会导致在作图分析中必须考虑的相关动物之间的多基因协方差。多样性近交(DO)小鼠在维持超过16代的多代繁殖设计中结合了八种创始菌株的遗传多样性。庞大的种群规模和随机交配确保了该种群的长期遗传稳定性。我们提出了一个完整的分析流程,用于在DO小鼠中进行基因作图,包括从基因型阵列强度数据中概率重建创始人单倍型的算法,以及适应多种创始人单倍型并说明动物之间相关性的作图方法。功效分析表明,仅用200只DO小鼠进行的研究就可以检测到效果显着的基因座,但是占性状变异<5%的基因座可能需要多达1000只动物的样本量。在免费提供的R包DOQTL中实现了此处描述的方法。

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