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MinYS:通过共生群落中的靶向基因组组装挖掘你的共生体。

MinYS: mine your symbiont by targeted genome assembly in symbiotic communities.

作者信息

Guyomar Cervin, Delage Wesley, Legeai Fabrice, Mougel Christophe, Simon Jean-Christophe, Lemaitre Claire

机构信息

Univ. Rennes, Inria, CNRS, IRISA, F-35000 Rennes, France.

Institut de Génétique, Environnement et Protection des Plantes (IGEPP), INRAE, Institut Agro, Univ. Rennes, F-35653 Le Rheu, France.

出版信息

NAR Genom Bioinform. 2020 Jul 3;2(3):lqaa047. doi: 10.1093/nargab/lqaa047. eCollection 2020 Sep.

Abstract

Most metazoans are associated with symbionts. Characterizing the effect of a particular symbiont often requires getting access to its genome, which is usually done by sequencing the whole community. We present MinYS, a targeted assembly approach to assemble a particular genome of interest from such metagenomic data. First, taking advantage of a reference genome, a subset of the reads is assembled into a set of backbone contigs. Then, this draft assembly is completed using the whole metagenomic readset in a manner. The resulting assembly is output as a genome graph, enabling different strains with potential structural variants coexisting in the sample to be distinguished. MinYS was applied to 50 pea aphid resequencing samples, with variable diversity in symbiont communities, in order to recover the genome sequence of its obligatory bacterial symbiont, . It was able to return high-quality assemblies (one contig assembly in 90% of the samples), even when using increasingly distant reference genomes, and to retrieve large structural variations in the samples. Because of its targeted essence, it outperformed standard metagenomic assemblers in terms of both time and assembly quality.

摘要

大多数后生动物都与共生体有关。表征特定共生体的作用通常需要获取其基因组,这通常通过对整个群落进行测序来完成。我们提出了MinYS,一种从这种宏基因组数据中组装特定目标基因组的靶向组装方法。首先,利用参考基因组,将一部分读段组装成一组骨架重叠群。然后,以一种方式使用整个宏基因组读段集来完成这个初步组装。最终的组装结果以基因组图谱的形式输出,从而能够区分样本中存在的具有潜在结构变异的不同菌株。MinYS应用于50个豌豆蚜重测序样本,这些样本的共生体群落具有不同的多样性,以便恢复其必需细菌共生体的基因组序列。即使使用距离越来越远的参考基因组,它也能够返回高质量的组装结果(90%的样本中为单重叠群组装),并检索样本中的大结构变异。由于其靶向本质,在时间和组装质量方面,它都优于标准的宏基因组组装程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7f/7671366/cf1b3edb851e/lqaa047fig1.jpg

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