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Development and Validation of a 20K Single Nucleotide Polymorphism (SNP) Whole Genome Genotyping Array for Apple (Malus × domestica Borkh)

机译:苹果(Malus×domestica Borkh)20K单核苷酸多态性(SNP)全基因组基因分型阵列的开发和验证

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摘要

High-density SNP arrays for genome-wide assessment of allelic variation have made high resolution genetic characterization of crop germplasm feasible. A medium density array for apple, the IRSC 8K SNP array, has been successfully developed and used for screens of bi-parental populations. However, the number of robust and well-distributed markers contained on this array was not sufficient to perform genome-wide association analyses in wider germplasm sets, or Pedigree-Based Analysis at high precision, because of rapid decay of linkage disequilibrium. We describe the development of an Illumina Infinium array targeting 20K SNPs. The SNPs were predicted from re-sequencing data derived from the genomes of 13 Malus × domestica apple cultivars and one accession belonging to a crab apple species (M. micromalus). A pipeline for SNP selection was devised that avoided the pitfalls associated with the inclusion of paralogous sequence variants, supported the construction of robust multi-allelic SNP haploblocks and selected up to 11 entries within narrow genomic regions of ±5 kb, termed focal points (FPs). Broad genome coverage was attained by placing FPs at 1 cM intervals on a consensus genetic map, complementing them with FPs to enrich the ends of each of the chromosomes, and by bridging physical intervals greater than 400 Kbps. The selection also included ∼3.7K validated SNPs from the IRSC 8K array. The array has already been used in other studies where ∼15.8K SNP markers were mapped with an average of ∼6.8K SNPs per full-sib family. The newly developed array with its high density of polymorphic validated SNPs is expected to be of great utility for Pedigree-Based Analysis and Genomic Selection. It will also be a valuable tool to help dissect the genetic mechanisms controlling important fruit quality traits, and to aid the identification of marker-trait associations suitable for the application of Marker Assisted Selection in apple breeding programs.
机译:用于等位基因变异的全基因组评估的高密度SNP阵列使作物种质的高分辨率遗传表征成为可能。苹果的中等密度阵列IRSC 8 K SNP阵列已成功开发,并用于双亲群体的筛选。然而,由于键合不平衡的快速衰减,该阵列上包含的坚固且分布均匀的标记物的数量不足以在更广泛的种质集中进行全基因组关联分析,或以高精度进行基于谱系的分析。我们描述了针对20 K个SNP的Illumina Infinium阵列的开发。根据从13个苹果属苹果属苹果品种和一个山楂苹果属(M. micromalus)的基因组中获得的重测序数据预测SNP。设计了SNP选择管道,避免了与包含同源序列变体相关的陷阱,支持构建稳健的多等位基因SNP单倍体,并在±5 kb的狭窄基因组区域内选择了多达11个条目,称为焦点(FPs) )。通过将FP以1 cM的间隔放置在共有遗传图谱上,用FP对其进行补充以丰富每个染色体的末端,并桥接大于400 Kbps的物理间隔,从而实现了广泛的基因组覆盖。选择还包括来自IRSC 8 K阵列的约3.7 K个经过验证的SNP。该阵列已经被用于其他研究中,其中〜15.8 K个SNP标记与每个全同胞家族平均约6.8 个K SNP进行了映射。新开发的阵列具有高密度的多态验证单核苷酸多态性,有望在基于谱系的分析和基因组选择中发挥巨大作用。这也将是一个有价值的工具,有助于剖析控制重要果实品质性状的遗传机制,并有助于鉴定适合于在苹果育种计划中应用标记辅助选择的标记-性状关联。

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