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Bioinformatics strategies for taxonomy independent binning and visualization of sequences in shotgun metagenomics

机译:生物信息学策略,用于shot子基因组学中的分类学独立分类和序列可视化

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摘要

One of main steps in a study of microbial communities is resolving their composition, diversity and function. In the past, these issues were mostly addressed by the use of amplicon sequencing of a target gene because of reasonable price and easier computational postprocessing of the bioinformatic data. With the advancement of sequencing techniques, the main focus shifted to the whole metagenome shotgun sequencing, which allows much more detailed analysis of the metagenomic data, including reconstruction of novel microbial genomes and to gain knowledge about genetic potential and metabolic capacities of whole environments. On the other hand, the output of whole metagenomic shotgun sequencing is mixture of short DNA fragments belonging to various genomes, therefore this approach requires more sophisticated computational algorithms for clustering of related sequences, commonly referred to as sequence binning. There are currently two types of binning methods: taxonomy dependent and taxonomy independent. The first type classifies the DNA fragments by performing a standard homology inference against a reference database, while the latter performs the reference-free binning by applying clustering techniques on features extracted from the sequences. In this review, we describe the strategies within the second approach. Although these strategies do not require prior knowledge, they have higher demands on the length of sequences. Besides their basic principle, an overview of particular methods and tools is provided. Furthermore, the review covers the utilization of the methods in context with the length of sequences and discusses the needs for metagenomic data preprocessing in form of initial assembly prior to binning.
机译:研究微生物群落的主要步骤之一是解决它们的组成,多样性和功能。过去,由于价格合理且生物信息数据的计算后处理更加简便,这些问题大多通过使用靶基因的扩增子测序来解决。随着测序技术的进步,主要重点转移到了整个元基因组shot弹枪测序上,从而可以对宏基因组学数据进行更详细的分析,包括重建新的微生物基因组,并获得有关整个环境的遗传潜力和代谢能力的知识。另一方面,整个宏基因组shot弹枪测序的输出是属于各种基因组的短DNA片段的混合物,因此,此方法需要更复杂的计算算法来对相关序列进行聚类,通常称为序列合并。当前有两种类型的分箱方法:与分类法相关和与分类法无关。第一种通过对参考数据库执行标准同源性推断来对DNA片段进行分类,而后一种通过对从序列中提取的特征应用聚类技术来执行无参考装仓。在这篇综述中,我们描述了第二种方法中的策略。尽管这些策略不需要先验知识,但是它们对序列的长度有更高的要求。除了其基本原理外,还提供了特定方法和工具的概述。此外,本综述涵盖了序列长度情况下方法的利用,并讨论了在装仓之前以初始组装形式进行宏基因组学数据预处理的需求。

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