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CrossMap: a versatile tool for coordinate conversion between genome assemblies.

机译:CrossMap:用于基因组装配之间坐标转换的多功能工具。

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MOTIVATION: Reference genome assemblies are subject to change and refinement from time to time. Generally, researchers need to convert the results that have been analyzed according to old assemblies to newer versions, or vice versa, to facilitate meta-analysis, direct comparison, data integration and visualization. Several useful conversion tools can convert genome interval files in browser extensible data or general feature format, but none have the functionality to convert files in sequence alignment map or BigWig format. This is a significant gap in computational genomics tools, as these formats are the ones most widely used for representing high-throughput sequencing data, such as RNA-seq, chromatin immunoprecipitation sequencing, DNA-seq, etc. RESULTS: Here we developed CrossMap, a versatile and efficient tool for converting genome coordinates between assemblies. CrossMap supports most of the commonly used file formats, including BAM, sequence alignment map, Wiggle, BigWig, browser extensible data, general feature format, gene transfer format and variant call format. AVAILABILITY AND IMPLEMENTATION: CrossMap is written in Python and C. Source code and a comprehensive user's manual are freely available at: http://crossmap.sourceforge.net/.
机译:动机:参考基因组组装会不时变化和完善。通常,研究人员需要将根据旧程序集分析的结果转换为较新的版本,反之亦然,以方便进行元分析,直接比较,数据集成和可视化。有几种有用的转换工具可以将基因组间隔文件转换为浏览器可扩展的数据或通用特征格式,但是没有一个工具可以转换序列比对图或BigWig格式的文件。这是计算基因组学工具中的一个重大空白,因为这些格式是最广泛用于表示高通量测序数据的格式,例如RNA-seq,染色质免疫沉淀测序,DNA-seq等。结果:在这里,我们开发了CrossMap,一种用于在装配之间转换基因组坐标的通用且高效的工具。 CrossMap支持大多数常用的文件格式,包括BAM,序列比对图,Wiggle,BigWig,浏览器可扩展数据,通用特征格式,基因转移格式和变异调用格式。可用性和实现:CrossMap用Python和C编写。源代码和全面的用户手册可从以下网址免费获得:http://crossmap.sourceforge.net/。

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