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New insights on Pseudoalteromonas haloplanktis TAC125 genome organization and benchmarks of genome assembly applications using next and third generation sequencing technologies

机译:使用下一个和第三代排序技术对伪阶霍普拉斯霍普拉斯坦的新见解霍普拉斯图TAC125基因组组织和基因组组装应用的基准

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Pseudoalteromonas haloplanktis TAC125 is among the most commonly studied bacteria adapted to cold environments. Aside from its ecological relevance, P. haloplanktis has a potential use for biotechnological applications. Due to its importance, we decided to take advantage of next generation sequencing (Illumina) and third generation sequencing (PacBio and Oxford Nanopore) technologies to resequence its genome. The availability of a reference genome, obtained using whole genome shotgun sequencing, allowed us to study and compare the results obtained by the different technologies and draw useful conclusions for future de novo genome assembly projects. We found that assembly polishing using Illumina reads is needed to achieve a consensus accuracy over 99.9% when using Oxford Nanopore sequencing, but not in PacBio sequencing. However, the dependency of consensus accuracy on coverage is lower in Oxford Nanopore than in PacBio, suggesting that a cost-effective solution might be the use of low coverage Oxford Nanopore sequencing together with Illumina reads. Despite the differences in consensus accuracy, all sequencing technologies revealed the presence of a large plasmid, pMEGA, which was undiscovered until now. Among the most interesting features of pMEGA is the presence of a putative error-prone polymerase regulated through the SOS response. Aside from the characterization of the newly discovered plasmid, we confirmed the sequence of the small plasmid pMtBL and uncovered the presence of a potential partitioning system. Crucially, this study shows that the combination of next and third generation sequencing technologies give us an unprecedented opportunity to characterize our bacterial model organisms at a very detailed level.
机译:假核霍乱卤代菌TAC125是适应冷环境的最常见的细菌之一。除了其生态相关性,P. Haloplanktis对生物技术应用潜在使用。由于其重要性,我们决定利用下一代测序(Illumina)和第三代测序(PACBIO和牛津纳米孔)技术来重新排序其基因组。使用全基因组霰弹枪测序获得的参考基因组的可用性使我们能够研究并比较不同技术获得的结果,并为未来的De Novo基因组装配项目绘制有用的结论。我们发现,需要使用Illumina读取的装配抛光,以在使用牛津纳米孔测序时获得超过99.9%的共识准确性,但不在PACBIO测序中。然而,共识精度对覆盖范围的依赖性比PACBIO在牛津纳米孔中较低,这表明一种成本效益的解决方案可能是使用低覆盖牛津纳米孔测序与Illumina读数一起使用。尽管差异共识准确,但所有测序技术都揭示了大质粒的PMEGA,直到现在。 PMEGA最有趣的特征是存在通过SOS反应调节推定的易易易用的聚合酶。除了新发现的质粒的表征外,我们证实了小质粒PMTBL的序列,并揭示了潜在分区系统的存在。这项研究表明,下一个和第三代排序技术的组合给了我们一个前所未有的机会,以在非常详细的水平下表征我们的细菌模型生物。

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