Tsiliki Georgia, Tsaramirsis Konstantinos, Kossida Sophia
Bioinformatics and Medical Informatics Team, Biomedical Research Foundation, Academy of Athens, 115 27 Athens, Greece.
Bioinformatics and Medical Informatics Team, Biomedical Research Foundation, Academy of Athens, 115 27 Athens, Greece ; Henley Business School, Business Informatics, University of Reading, Whiteknights, Reading RG6 6UD, Uk.
Biomed Res Int. 2014;2014:893501. doi: 10.1155/2014/893501. Epub 2014 May 20.
The past years have shown an enormous advancement in sequencing and array-based technologies, producing supplementary or alternative views of the genome stored in various formats and databases. Their sheer volume and different data scope pose a challenge to jointly visualize and integrate diverse data types. We present AmalgamScope a new interactive software tool focusing on assisting scientists with the annotation of the human genome and particularly the integration of the annotation files from multiple data types, using gene identifiers and genomic coordinates. Supported platforms include next-generation sequencing and microarray technologies. The available features of AmalgamScope range from the annotation of diverse data types across the human genome to integration of the data based on the annotational information and visualization of the merged files within chromosomal regions or the whole genome. Additionally, users can define custom transcriptome library files for any species and use the file exchanging distant server options of the tool.
过去几年,测序技术和基于阵列的技术取得了巨大进展,产生了以各种格式存储在不同数据库中的基因组的补充或替代视图。它们庞大的数据量和不同的数据范围对联合可视化和整合不同数据类型构成了挑战。我们展示了AmalgamScope,这是一种新的交互式软件工具,专注于协助科学家对人类基因组进行注释,特别是使用基因标识符和基因组坐标整合来自多种数据类型的注释文件。支持的平台包括下一代测序和微阵列技术。AmalgamScope的可用功能范围从对整个人类基因组的各种数据类型进行注释,到基于注释信息整合数据,以及在染色体区域或整个基因组内可视化合并文件。此外,用户可以为任何物种定义自定义转录组文库文件,并使用该工具的文件交换远程服务器选项。