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A highly flexible and repeatable genotyping method for aquaculture studies based on target amplicon sequencing using next-generation sequencing technology

机译:一种基于水产养殖研究的高度灵活且可重复的基因分型方法该方法基于目标扩增子测序并使用下一代测序技术

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摘要

Studies using genome-wide single nucleotide polymorphisms (SNPs) have become commonplace in genetics and genomics, due to advances in high-throughput sequencing technologies. Since the numbers of required SNPs and samples vary depending on each research goal, genotyping technologies with high flexibility in the number of SNPs/samples and high repeatability have been intensively investigated. For example, the ultrahigh-multiplexed amplicon sequencing, Ion AmpliSeq, has been used as a high-throughput genotyping method mainly for diagnostic purposes. Here, we designed a custom panel targeting 3,187 genome-wide SNPs of fugu, Takifugu rubripes, and applied it for genotyping farmed fugu to test its feasibility in aquaculture studies. We sequenced two libraries consisting of different pools of individuals (n = 326 each) on the Illumina MiSeq sequencer. Consequently, over 99% target regions (3,178 SNPs) were amplified and 2,655 SNPs were available after filtering steps. Strong correlation was observed in the mean depth of coverage of each SNP between duplicate runs (r = 0.993). Genetic analysis using these genotype data successfully detected the known population structure and the sex determining locus of fugu. These results show the method is superior in repeatability and flexibility, and suits genetic studies including molecular breeding, such as marker assisted and genomic selection.
机译:由于高通量测序技术的进步,使用全基因组单核苷酸多态性(SNP)的研究已在遗传学和基因组学领域变得司空见惯。由于所需的SNP和样品的数量根据每个研究目标而变化,因此对SNP /样品的数量具有高度灵活性和高重复性的基因分型技术进行了深入研究。例如,超高倍扩增子测序,Ion AmpliSeq,已被用作主要用于诊断目的的高通量基因分型方法。在这里,我们设计了一个针对3,187个全基因型河豚鱼(Takifugu rubripes)全基因组SNP的定制面板,并将其用于养殖河豚的基因分型,以测试其在水产养殖研究中的可行性。我们在Illumina MiSeq测序仪上测序了两个由不同的个体库组成的文库(每个n = 326)。因此,在过滤步骤后,超过99%的目标区域(3,178个SNP)被扩增,并且2,655个SNP可用。在两次重复之间,每个SNP的平均覆盖深度观察到强相关性(r(= 0.993)。使用这些基因型数据进行的遗传分析成功地检测出了河豚的已知种群结构和性别决定基因座。这些结果表明该方法具有良好的重复性和灵活性,适用于包括分子育种在内的遗传研究,例如标记辅助和基因组选择。

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