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Construction of a SNP-based genetic linkage map in cultivated peanut based on large scale marker development using next-generation double-digest restriction-site-associated DNA sequencing (ddRADseq)

机译:基于下一代双消化限制性位点相关DNA测序(ddRADseq)的大规模标记开发在栽培花生中构建基于SNP的遗传连锁图谱

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摘要

BackgroundCultivated peanut, or groundnut (Arachis hypogaea L.), is an important oilseed crop with an allotetraploid genome (AABB, 2n = 4x = 40). In recent years, many efforts have been made to construct linkage maps in cultivated peanut, but almost all of these maps were constructed using low-throughput molecular markers, and most show a low density, directly influencing the value of their applications. With advances in next-generation sequencing (NGS) technology, the construction of high-density genetic maps has become more achievable in a cost-effective and rapid manner. The objective of this study was to establish a high-density single nucleotide polymorphism (SNP)-based genetic map for cultivated peanut by analyzing next-generation double-digest restriction-site-associated DNA sequencing (ddRADseq) reads.
机译:背景栽培花生或花生(花生)是一种重要的油菜作物,具有异源四倍体基因组(AABB,2n == 4x == 40)。近年来,已经做出了很多努力来在栽培花生中构建连锁图,但是几乎所有这些图都是使用低通量分子标记构建的,并且大多数都显示出低密度,直接影响了其应用价值。随着下一代测序(NGS)技术的进步,高密度遗传图谱的构建已经变得更加经济高效。这项研究的目的是通过分析下一代双消化的限制性位点相关的DNA测序(ddRADseq)读数,为栽培花生建立基于高密度单核苷酸多态性(SNP)的遗传图谱。

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