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Whole genome resequencing of tobacco (Nicotiana tabacum L.) genotypes and high-throughput SNP discovery

机译:烟草(尼古利亚纳Tabacum L.)基因型和高通量SNP发现的全基因组重新开始

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摘要

Genome-wide single-nucleotide polymorphisms (SNPs) are highly useful in unraveling genetic insights and are essential to accelerate selections for genetic improvement in tobacco. The discovery of genome-wide SNPs in tobacco is very complex due to its high level of repetitive genome and polyploidy. At present, publicly available genomic data on SNPs are very limited, which warrants the need for high-throughput SNPs for application in tobacco breeding. In this research paper, we describe our efforts on SNP discovery by whole genome resequencing of 18 flue-cured Virginia (FCV) tobacco genotypes and annotation of SNPs in the tobacco genome. A large amount of data of about 225GB per genotype was generated, with an average read depth of 50x using paired-end next-generation sequencing (NGS) with the HiSeq 2500 platform. The discovery of a large number of SNPs and indels was attempted to assist mapping and, thus, the selection processes to develop superior tobacco breeding lines. Discovered SNPs, their functional annotation, mapping to the reference genome, and their relative positioning in the linkage group are discussed in this paper.
机译:基因组 - 宽的单核苷酸多态性(SNP)在解开遗传识别方面非常有用,并且对于加速烟草遗传改善的选择是必不可少的。由于其高水平的重复基因组和多倍体,在烟草中发现基因组SNP是非常复杂的。目前,SNP上的公开可用的基因组数据非常有限,这是对高通量SNP的需求进行烟草繁殖中的应用。在本研究论文中,我们描述了我们在烟草基因组中的18个烤常年(FCV)烟草基因型和SNP的注释来描述我们对SNP Discovery的努力。产生每种基因型约225gB的大量数据,使用与Hiseq 2500平台的配对结束的下一代测序(NGS)平均读取深度为50倍。尝试发现大量SNP和Indels,以帮助映射,从而进行选择过程,以开发出优越的烟草繁殖线。发现SNP,它们的功能注释,映射到参考基因组,以及它们在连锁组中的相对定位在本文中。

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