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Next Generation Semiconductor Based Sequencing of the Donkey (Equus asinus) Genome Provided Comparative Sequence Data against the Horse Genome and a Few Millions of Single Nucleotide Polymorphisms

机译:驴(马属)基因组的下一代基于半导体的测序提供了针对马基因组和数百万个单核苷酸多态性的比较序列数据

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摘要

Few studies investigated the donkey (Equus asinus) at the whole genome level so far. Here, we sequenced the genome of two male donkeys using a next generation semiconductor based sequencing platform (the Ion Proton sequencer) and compared obtained sequence information with the available donkey draft genome (and its Illumina reads from which it was originated) and with the EquCab2.0 assembly of the horse genome. Moreover, the Ion Torrent Personal Genome Analyzer was used to sequence reduced representation libraries (RRL) obtained from a DNA pool including donkeys of different breeds (Grigio Siciliano, Ragusano and Martina Franca). The number of next generation sequencing reads aligned with the EquCab2.0 horse genome was larger than those aligned with the draft donkey genome. This was due to the larger N50 for contigs and scaffolds of the horse genome. Nucleotide divergence between E. caballus and E. asinus was estimated to be ~ 0.52-0.57%. Regions with low nucleotide divergence were identified in several autosomal chromosomes and in the whole chromosome X. These regions might be evolutionally important in equids. Comparing Y-chromosome regions we identified variants that could be useful to track donkey paternal lineages. Moreover, about 4.8 million of single nucleotide polymorphisms (SNPs) in the donkey genome were identified and annotated combining sequencing data from Ion Proton (whole genome sequencing) and Ion Torrent (RRL) runs with Illumina reads. A higher density of SNPs was present in regions homologous to horse chromosome 12, in which several studies reported a high frequency of copy number variants. The SNPs we identified constitute a first resource useful to describe variability at the population genomic level in E. asinus and to establish monitoring systems for the conservation of donkey genetic resources.
机译:到目前为止,很少有研究在整个基因组水平上研究驴(Equus asinus)。在这里,我们使用下一代基于半导体的测序平台(离子质子测序仪)对两个雄性驴的基因组进行了测序,并将获得的序列信息与可用的驴吃草基因组(及其起源的Illumina读物)以及EquCab2进行了比较。 .0马基因组的组装。此外,离子激流个人基因组分析仪用于对从包括不同品种的驴(Grigio Siciliano,Ragusano和Martina Franca)的DNA池中获得的简化表示文库(RRL)进行测序。与EquCab2.0马基因组比对的下一代测序读数的数目大于与驴基因组比对的读数。这是由于马基因组的重叠群和支架的N50较大。 E. caballus和A. asinus之间的核苷酸差异估计为〜0.52-0.57%。在几个常染色体和整个X染色体中都鉴定出了核苷酸差异低的区域。这些区域可能在进化上具有重要的意义。比较Y染色体区域,我们确定了可用于跟踪驴父本世系的变体。此外,在驴基因组中鉴定并注释了约480万个单核苷酸多态性(SNP),并结合了来自Ilon质子的测序数据(全基因组测序)和Ionlumina读取的Ion Torrent(RRL)序列。在与马12号染色体同源的区域中存在更高密度的SNP,其中一些研究报告了高拷贝数变异体的频率。我们鉴定出的SNP构成了第一个资源,可用于描述中华绒螯蟹种群基因组水平的变异性,并建立保护驴遗传资源的监测系统。

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