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Genome skimming is a low-cost and robust strategy to assemble complete mitochondrial genomes from ethanol preserved specimens in biodiversity studies

机译:基因组撇渣是一种低成本和稳健的策略,用于组装来自生物多样性研究中的乙醇保存标本的完全线粒体基因组

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摘要

Global loss of biodiversity is an ongoing process that concerns both local and global authorities. Studies of biodiversity mainly involve traditional methods using morphological characters and molecular protocols. However, conventional methods are a time consuming and resource demanding task. The development of high-throughput sequencing (HTS) techniques has reshaped the way we explore biodiversity and opened a path to new questions and novel empirical approaches. With the emergence of HTS, sequencing the complete mitochondrial genome became more accessible, and the number of genome sequences published has increased exponentially during the last decades. Despite the current state of knowledge about the potential of mitogenomics in phylogenetics, this is still a relatively under-explored area for a multitude of taxonomic groups, especially for those without commercial relevance, non-models organisms and with preserved DNA. Here we take the first step to assemble and annotate the genomes from HTS data using a new protocol of genome skimming which will offer an opportunity to extend the field of mitogenomics to under-studied organisms. We extracted genomic DNA from specimens preserved in ethanol. We used Nextera XT DNA to prepare indexed paired-end libraries since it is a powerful tool for working with diverse samples, requiring a low amount of input DNA. We sequenced the samples in two different Illumina platform (MiSeq or NextSeq 550). We trimmed raw reads, filtered and had their quality tested accordingly. We performed the assembly using a baiting and iterative mapping strategy, and the annotated the putative mitochondrion through a semi-automatic procedure. We applied the contiguity index to access the completeness of each new mitogenome. Our results reveal the efficiency of the proposed method to recover the whole mitogenomes of preserved DNA from non-model organisms even if there are gene rearrangement in the specimens. Our findings suggest the potential of combining the adequate platform and library to the genome skimming as an innovative approach, which opens a new range of possibilities of its use to obtain molecular data from organisms with different levels of preservation.
机译:全球生物多样性丧失是一个持续的过程,涉及本地和全球当局。生物多样性的研究主要涉及使用形态特征和分子方案的传统方法。然而,传统方法是耗时和资源要求的任务。高通量测序(HTS)技术的开发重塑了我们探索生物多样性的方式,并开启了新问题和新型实证方法的道路。随着HTS的出现,测序完全线粒体基因组变得更加接近,并且出版的基因组序列的数量在过去几十年中呈指数增加。尽管目前有关系统源性毒性学潜力的潜力的知识状态,但仍然是众多分类学团体的探索区域,特别是对于没有商业相关性的人,非模型生物和保存的DNA。在这里,我们采取第一步来组装和注释来自HTS数据的基因组,使用新的基因组撇杀协议将提供延伸诱导毒物学领域的机会,以便在学习的生物体中扩展。我们从保存在乙醇中的样品中提取基因组DNA。我们使用Nextera XT DNA准备索引配对终端库,因为它是一种用于使用不同样品的强大工具,需要少量输入DNA。我们在两个不同的Illumina平台(Miseq或Nextseq 550)中测序样本。我们修剪了原始读取,过滤并相应地测试了质量。我们使用诱饵和迭代映射策略进行了组装,并通过半自动过程注释推定的线粒体。我们施加了恒星指数来访问每个新发丝器的完整性。我们的结果揭示了所提出的方法,即使样品中存在基因重排,所以拟议的方法恢复保存的DNA的整个毒蛛。我们的研究结果表明,将足够的平台和图书馆结合到基因组撇去作为一种创新方法的可能性,这为其用于从具有不同保存水平的生物体的分子数据开辟了新的可能性。

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