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GenomeRing: alignment visualization based on SuperGenome coordinates

机译:GenomeRing:基于SuperGenome坐标的比对可视化

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摘要

>Motivation: The number of completely sequenced genomes is continuously rising, allowing for comparative analyses of genomic variation. Such analyses are often based on whole-genome alignments to elucidate structural differences arising from insertions, deletions or from rearrangement events. Computational tools that can visualize genome alignments in a meaningful manner are needed to help researchers gain new insights into the underlying data. Such visualizations typically are either realized in a linear fashion as in genome browsers or by using a circular approach, where relationships between genomic regions are indicated by arcs. Both methods allow for the integration of additional information such as experimental data or annotations. However, providing a visualization that still allows for a quick and comprehensive interpretation of all important genomic variations together with various supplemental data, which may be highly heterogeneous, remains a challenge.>Results: Here, we present two complementary approaches to tackle this problem. First, we propose the SuperGenome concept for the computation of a common coordinate system for all genomes in a multiple alignment. This coordinate system allows for the consistent placement of genome annotations in the presence of insertions, deletions and rearrangements. Second, we present the GenomeRing visualization that, based on the SuperGenome, creates an interactive overview visualization of the multiple genome alignment in a circular layout. We demonstrate our methods by applying them to an alignment of Campylobacter jejuni strains for the discovery of genomic islands as well as to an alignment of Helicobacter pylori, which we visualize in combination with gene expression data.>Availability: GenomeRing and example data is available at >Contact:
机译:>动机:完全测序的基因组数量不断增加,可以对基因组变异进行比较分析。此类分析通常基于全基因组比对,以阐明由于插入,缺失或重排事件引起的结构差异。需要能够以有意义的方式可视化基因组比对的计算工具,以帮助研究人员获得对基础数据的新见解。这样的可视化通常或者以在基因组浏览器中的线性方式来实现,或者通过使用圆形方法来实现,其中通过弧线指示基因组区域之间的关系。两种方法都允许集成其他信息,例如实验数据或注释。但是,提供可视化方法仍然可以快速,全面地解释所有重要的基因组变异以及各种补充数据,这些数据可能是高度异质的,这仍然是一个挑战。>结果:在这里,我们提出两种互补的方法解决这个问题的方法。首先,我们提出了SuperGenome概念,用于计算多重比对中所有基因组的公共坐标系。该坐标系允许在插入,缺失和重排的情况下基因组注释的一致放置。其次,我们介绍了GenomeRing可视化,该可视化基于SuperGenome,以环形布局创建了多个基因组比对的交互式概览可视化。我们通过将它们应用于空肠弯曲杆菌菌株的比对以发现基因组岛以及幽门螺杆菌的比对来证明我们的方法,我们结合基因表达数据对其进行可视化。>可用性: GenomeRing并且示例数据可从>联系人:获得

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