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MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation

机译:MagicViewer:用于下一代测序数据可视化以及遗传变异检测和注释的集成解决方案

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New sequencing technologies, such as Roche 454, ABI SOLiD and Illumina, have been increasingly developed at an astounding pace with the advantages of high throughput, reduced time and cost. To satisfy the impending need for deciphering the large-scale data generated from next-generation sequencing, an integrated software MagicViewer is developed to easily visualize short read mapping, identify and annotate genetic variation based on the reference genome. MagicViewer provides a user-friendly environment in which large-scale short reads can be displayed in a zoomable interface under user-defined color scheme through an operating system-independent manner. Meanwhile, it also holds a versatile computational pipeline for genetic variation detection, filtration, annotation and visualization, providing details of search option, functional classification, subset selection, sequence association and primer design. In conclusion, MagicViewer is a sophisticated assembly visualization and genetic variation annotation tool for next-generation sequencing data, which can be widely used in a variety of sequencing-based researches, including genome re-sequencing and transcriptome studies. MagicViewer is freely available at http://bioinformatics.zj.cn/magicviewer/.
机译:新的测序技术,例如Roche 454,ABI SOLiD和Illumina,以惊人的速度不断发展,具有高通量,减少时间和成本的优势。为了满足破译下一代测序所产生的大规模数据的迫切需求,开发了集成软件MagicViewer,可以轻松地可视化短读图谱,基于参考基因组识别和注释遗传变异。 MagicViewer提供了一种用户友好的环境,在该环境中,可以通过独立于操作系统的方式在用户定义的配色方案下以可缩放的界面显示大规模的短读。同时,它还拥有用于遗传变异检测,过滤,注释和可视化的通用计算流水线,提供了搜索选项,功能分类,子集选择,序列关联和引物设计的详细信息。总之,MagicViewer是用于下一代测序数据的复杂的装配可视化和遗传变异注释工具,可广泛用于各种基于测序的研究,包括基因组重测序和转录组研究。 MagicViewer可从http://bioinformatics.zj.cn/magicviewer/免费获得。

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