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Anchored Hybrid Enrichment for Massively High-Throughput Phylogenomics

机译:大规模高通量系统学的锚定杂化富集

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摘要

The field of phylogenetics is on the cusp of a major revolution, enabled by new methods of data collection that leverage both genomic resources and recent advances in DNA sequencing. Previous phylogenetic work has required labor-intensive marker development coupled with single-locus polymerase chain reaction and DNA sequencing on clade-by-clade and locus-by-locus basis. Here, we present a new, cost-efficient, and rapid approach to obtaining data from hundreds of loci for potentially hundreds of individuals for deep and shallow phylogenetic studies. Specifically, we designed probes for target enrichment of 500 loci in highly conserved anchor regions of vertebrate genomes (flanked by less conserved regions) from five model species and tested enrichment efficiency in nonmodel species up to 508 million years divergent from the nearest model. We found that hybrid enrichment using conserved probes (anchored enrichment) can recover a large number of unlinked loci that are useful at a diversity of phylogenetic timescales. This new approach has the potential not only to expedite resolution of deep-scale portions of the Tree of Life but also to greatly accelerate resolution of the large number of shallow clades that remain unresolved. The combination of low cost (∼1% of the cost of traditional Sanger sequencing and ∼3.5% of the cost of high-throughput amplicon sequencing for projects on the scale of 500 loci × 100 individuals) and rapid data collection (∼2 weeks of laboratory time) are expected to make this approach tractable even for researchers working on systems with limited or nonexistent genomic resources.
机译:系统发育学领域正处于一场重大革命的风口浪尖上,这得益于利用基因组资源和DNA测序的最新进展的新数据收集方法。以前的系统进化工作要求劳动密集型标记的开发,以及单基因座聚合酶链反应和逐个基因座和逐个基因座的基础上的DNA测序。在这里,我们提出了一种新的,具有成本效益的,快速的方法,可以从数百个基因座中获取潜在的数百个个体的数据,以进行深层和浅层系统发育研究。具体而言,我们设计了探针,用于从五个模型物种中高度保守的脊椎动物基因组锚定区域(侧翼为保守性较低的区域)中富集超过500个基因座的探针,并测试了从最近的模型到5.08亿年的非模型物种的富集效率。我们发现使用保守探针的杂交富集(锚定富集)可以回收大量未连锁的基因座,这些基因座在各种系统发生时间尺度上都是有用的。这种新方法不仅有可能加快生命之树深层部分的分辨率,而且有可能大大加快尚未解决的大量浅枝的分辨率。低成本(传统Sanger测序成本的约1%,高通量扩增子测序成本的约3.5%,规模为500个基因座×100个人的项目)与快速数据收集(约2周)的结合即使对于使用有限或不存在基因组资源的系统进行研究的研究人员,也有望使这种方法易于处理。

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  • 来源
    《Systematic Biology》 |2012年第5期|p.727-744|共18页
  • 作者单位

    1 Department of Scientific Computing, Florida State University, Dirac Science Library, Tallahassee, FL 32306-4102, USA;

    and 2 Department of Biological Science, Florida State University, 319 Stadium Drive, PO Box 3064295, Tallahassee, FL, 32306-4295, USA;

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