利用本体可视化协调人类疾病基因的跨物种功能标注

M. Dolan, J. Blake
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引用次数: 7

摘要

生物医学本体为支持生物知识的整合和检索提供了表征系统。基因本体(GO)被广泛用于基因的分子属性标注,为比较功能分析研究提供了一种通用范式。扩展任何一个基因产物的功能的一种方法是比较具有密切进化关系和可能以相似方式起作用的基因的注释,例如同源基因。我们正在探索GO和orthology集合的力量,通过在本体关系结构中呈现可视化的注释,提供跨物种协调的注释的全面视图。这项工作描述了我们的本体可视化方法在一组与人类疾病基因同源的模式生物基因中的应用
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using Ontology Visualization to Coordinate Cross-species Functional Annotation for Human Disease Genes
Biomedical ontologies provide representational system to support the integration and retrieval of biological knowledge. The gene ontology (GO) is widely used to annotate molecular attributes of genes and provides a common paradigm for comparative functional analysis research. One way to expand the view of the function of any one gene product is to compare annotations of genes that share close evolutionary relationships and are likely to function in similar ways, such as orthologous genes. We are exploring the power of the GO and orthology sets to provide a comprehensive view of annotations coordinated across species by presenting annotations visualized within the ontology relationship structure. This work describes the application of our ontology visualization approach to a set of model organism genes that are orthologous to human disease genes
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