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Phylogenetic understanding of clonal populations in an era of whole genome sequencing

机译:全基因组测序时代对克隆种群的系统发生学理解

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Phylogenetic hypotheses using whole genome sequences have the potential for unprecedented accuracy, yet a failure to understand issues associated with discovery bias, character sampling, and strain sampling can lead to highly erroneous conclusions. For microbial pathogens, phylogenies derived from whole genome sequences are becoming more common, as large numbers of characters distributed across entire genomes can yield extremely accurate phylogenies, particularly for strictly clonal populations. The availability of whole genomes is increasing as new sequencing technologies reduce the cost and time required for genome sequencing. Until entire sample collections can be fully sequenced, harnessing the phylogenetic power from whole genome sequences in more than a small subset of fully sequenced strains requires the integration of whole genome and partial genome genotyping data. Such integration involves discovering evolutionarily stable polymorphic characters by whole genome comparisons, then determining allelic states across a wide panel of isolates using high-throughput genotyping technologies. Here, we demonstrate how such an approach using single nucleotide polymorphisms (SNPs) yields highly accurate, but biased phylogenetic reconstructions and how the accuracy of the resulting tree is compromised by incomplete taxon and character sampling. Despite recent phylogenetic work detailing the strengths and biases of integrating whole genome and partial genome genotype data, these issues are relatively new and remain poorly understood by many researchers. Here, we revisit these biases and provide strategies for maximizing phylogenetic accuracy. Although we write this review with bacterial pathogens in mind, these concepts apply to any clonally reproducing population or indeed to any evolutionarily stable marker that is inherited in a strictly clonal manner. Understanding the ways in which current and emerging technologies can be used to maximize phylogenetic knowledge is advantageous only with a complete understanding of the strengths and weaknesses of these methods.
机译:使用全基因组序列的系统发育假说可能具有空前的准确性,但未能理解与发现偏倚,特征采样和应变采样相关的问题可能会导致高度错误的结论。对于微生物病原体,源自整个基因组序列的系统发育正变得越来越普遍,因为在整个基因组中分布的大量特征可以产生极其准确的系统发育,特别是对于严格的克隆种群而言。随着新的测序技术降低了基因组测序所需的成本和时间,整个基因组的可用性正在增加。在对整个样本收集物进行完全测序之前,要利用整个基因组序列的系统发育能力,而不是一小部分完全测序的菌株,就需要对整个基因组和部分基因组基因分型数据进行整合。这种整合包括通过全基因组比较发现进化上稳定的多态性特征,然后使用高通量基因分型技术在一系列分离物中确定等位基因状态。在这里,我们演示了使用单核苷酸多态性(SNP)的这种方法如何产生高度准确但有偏差的系统发育重建,以及如何通过不完整的分类和字符采样来损害生成树的准确性。尽管最近进行了系统进化研究,详细阐述了整合全基因组和部分基因组基因型数据的优势和偏见,但这些问题相对较新,许多研究人员对此知之甚少。在这里,我们重新审视这些偏差,并提供最大限度地提高系统发育准确性的策略。尽管我们在撰写本文时就牢记细菌病原体,但这些概念适用于任何克隆繁殖种群或确实适用于以严格克隆方式遗传的任何进化稳定标记。只有全面了解这些方法的优缺点,才能理解利用当前和新兴技术来最大化系统发育知识的方式。

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