Kim Changhoon
Bioinformatics Institute, Macrogen Inc., Seoul 08511, Korea.
BMB Rep. 2016 Dec;49(12):653-654. doi: 10.5483/bmbrep.2016.49.12.195.
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. [BMB Reports 2016; 49(12): 653-654].
由基因组参考联盟维护的人类参考基因组,可以说是自首次构建以来最完整的基因组组装。由于各种技术进步,通过纳入对先前组装的修正,它一直在不断改进。由于高通量测序技术最近的成熟,许多目前正在进行的群体测序项目都基于这个参考基因组,这增加了开发基因组信息有用医学应用的希望。然而,仅仅一个参考基因组并不适合全球所有人群,因为基因组结构存在很大差异以及短读测序方法固有的技术限制。最近通过将单分子技术与常规测序数据相结合,在不采用传统的逐个克隆测序和物理图谱绘制的情况下,成功地从头构建了高度连续的亚洲二倍体基因组AK1,通过检测数千个新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缺口,揭示了基因组结构变异的本质。现在预计,AK1基因组很快将与更多即将从头组装的基因组配对,这将为探索在群体基因组学中使用特定祖先参考基因组而非hg19/hg38的实际情况提供机会。这是朝着推进基于基因的精准医学迈出的重要一步。[《BMB报告》2016年;49(12):653 - 654]