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Birth of an ‘Asian cool’ reference genome: AK1

机译:亚洲酷参考基因组的诞生:AK1

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摘要

The human reference genome, maintained by the Genome Reference Consortium, is conceivably the most complete genome assembly ever, since its first construction. It has continually been improved by incorporating corrections made to the previous assemblies, thanks to various technological advances. Many currently-ongoing population sequencing projects have been based on this reference genome, heightening hopes of the development of useful medical applications of genomic information, thanks to the recent maturation of high-throughput sequencing technologies. However, just one reference genome does not fit all the populations across the globe, because of the large diversity in genomic structures and technical limitations inherent to short read sequencing methods. The recent success in de novo construction of the highly contiguous Asian diploid genome AK1, by combining single molecule technologies with routine sequencing data without resorting to traditional clone-by-clone sequencing and physical mapping, reveals the nature of genomic structure variation by detecting thousands of novel structural variations and by finally filling in some of the prior gaps which had persistently remained in the current human reference genome. Now it is expected that the AK1 genome, soon to be paired with more upcoming de novo assembled genomes, will provide a chance to explore what it is really like to use ancestry-specific reference genomes instead of hg19/hg38 for population genomics. This is a major step towards the furthering of genetically-based precision medicine.
机译:由基因组参考协会维护的人类参考基因组,自其首次构建以来,可能是有史以来最完整的基因组组装。由于各种技术的进步,通过合并对先前组件所做的更正,使其得到了不断改进。由于高通量测序技术的日趋成熟,许多当前正在进行的群体测序项目都基于该参考基因组,从而提高了开发基因组信息的有用医学应用的希望。然而,由于短读测序方法固有的基因组结构多样性和技术局限性,仅一个参考基因组无法适应全球所有人群。通过将单分子技术与常规测序数据结合而无需借助传统的逐个克隆测序和物理作图的方法,高度连续的亚洲二倍体基因组AK1在从头构建中的最新成功通过检测数千个ABC序列揭示了基因组结构变异的本质。新颖的结构变异,并最终填补了当前人类参考基因组中一直存在的一些先前的空白。现在,预计AK1基因组将很快与更多即将到来的从头组装基因组配对,这将为探索使用祖先特异性参考基因组而不是hg19 / hg38进行种群基因组学的真正机会提供机会。这是进一步发展基于基因的精密医学的重要一步。

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