Nakamura Yoji, Yasuike Motoshige, Nishiki Issei, Iwasaki Yuki, Fujiwara Atushi, Kawato Yasuhiko, Nakai Toshihiro, Nagai Satoshi, Kobayashi Takanori, Gojobori Takashi, Ototake Mitsuru
Research Center for Aquatic Genomics, National Research Institute of Fisheries Science, Fisheries Research Agency, 2-12-4 Fukuura, Kanazawa, Yokohama 236-8648, Kanagawa, Japan.
Research Center for Aquatic Genomics, National Research Institute of Fisheries Science, Fisheries Research Agency, 2-12-4 Fukuura, Kanazawa, Yokohama 236-8648, Kanagawa, Japan.
Gene. 2016 Feb 1;576(2 Pt 1):676-80. doi: 10.1016/j.gene.2015.10.029. Epub 2015 Oct 22.
Next-generation sequencing technologies have allowed the rapid determination of the complete genomes of many organisms. Although shotgun sequences from large genome organisms are still difficult to reconstruct perfect contigs each of which represents a full chromosome, those from small genomes have been assembled successfully into a very small number of contigs. In this study, we show that shotgun reads from phage genomes can be reconstructed into a single contig by controlling the number of read sequences used in de novo assembly. We have developed a pipeline to assemble small viral genomes with good reliability using a resampling method from shotgun data. This pipeline, named V-GAP (Viral Genome Assembly Pipeline), will contribute to the rapid genome typing of viruses, which are highly divergent, and thus will meet the increasing need for viral genome comparisons in metagenomic studies.
新一代测序技术已使快速测定许多生物的完整基因组成为可能。尽管来自大型基因组生物的鸟枪法序列仍难以重建出完美的重叠群(每个重叠群代表一条完整染色体),但来自小型基因组的序列已成功组装成数量极少的重叠群。在本研究中,我们表明,通过控制从头组装中使用的读段序列数量,噬菌体基因组的鸟枪法读段可被重建为单个重叠群。我们开发了一种流程,利用来自鸟枪法数据的重采样方法,以良好的可靠性组装小型病毒基因组。这个名为V-GAP(病毒基因组组装流程)的流程将有助于对高度多样化的病毒进行快速基因组分型,从而满足宏基因组学研究中对病毒基因组比较日益增长的需求。