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Low-depth genotyping-by-sequencing (GBS) in a bovine population: strategies to maximize the selection of high quality genotypes and the accuracy of imputation

机译:牛群中的低深度测序测序(GBS):最大化选择高质量基因型和估算准确性的策略

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摘要

BackgroundGenotyping-by-sequencing (GBS) has emerged as a powerful and cost-effective approach for discovering and genotyping single-nucleotide polymorphisms. The GBS technique was largely used in crop species where its low sequence coverage is not a drawback for calling genotypes because inbred lines are almost homozygous. In contrast, only a few studies used the GBS technique in animal populations (with sizeable heterozygosity rates) and many of those that have been published did not consider the quality of the genotypes produced by the bioinformatic pipelines. To improve the sequence coverage of the fragments, an alternative GBS preparation protocol that includes selective primers during the PCR amplification step has been recently proposed. In this study, we compared this modified protocol with the conventional two-enzyme GBS protocol. We also described various procedures to maximize the selection of high quality genotypes and to increase the accuracy of imputation.
机译:背景技术测序基因分型(GBS)已经成为一种发现和基因分型单核苷酸多态性的有力且具有成本效益的方法。 GBS技术主要用于农作物物种,其低序列覆盖率对于调用基因型不是不利的,因为自交系几乎是纯合的。相比之下,只有少数研究在动物种群中使用了GBS技术(具有相当大的杂合率),许多已发表的研究并未考虑生物信息学管道产生的基因型的质量。为了提高片段的序列覆盖率,最近提出了另一种GBS制备方案,该方案包括在PCR扩增步骤中选择的引物。在这项研究中,我们将修改后的协议与常规的两种酶GBS协议进行了比较。我们还描述了各种程序,以最大程度地选择高质量的基因型并增加插补的准确性。

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