Using semantic web rules to reason on an ontology of pseudogenes

被引:14
作者
Holford, Matthew E. [1 ]
Khurana, Ekta [2 ]
Cheung, Kei-Hoi [1 ,3 ,4 ,5 ]
Gerstein, Mark [1 ,2 ,3 ]
机构
[1] Yale Univ, Program Computat Biol & Bioinformat, New Haven, CT 06520 USA
[2] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[3] Yale Univ, Dept Comp Sci, New Haven, CT 06520 USA
[4] Yale Univ, Ctr Med Informat, New Haven, CT 06520 USA
[5] Yale Univ, Dept Genet, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
EVOLUTION; DATABASE;
D O I
10.1093/bioinformatics/btq173
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Recent years have seen the development of a wide range of biomedical ontologies. Notable among these is Sequence Ontology (SO) which offers a rich hierarchy of terms and relationships that can be used to annotate genomic data. Well-designed formal ontologies allow data to be reasoned upon in a consistent and logically sound way and can lead to the discovery of new relationships. The Semantic Web Rules Language (SWRL) augments the capabilities of a reasoner by allowing the creation of conditional rules. To date, however, formal reasoning, especially the use of SWRL rules, has not been widely used in biomedicine. Results: We have built a knowledge base of human pseudogenes, extending the existing SO framework to incorporate additional attributes. In particular, we have defined the relationships between pseudogenes and segmental duplications. We then created a series of logical rules using SWRL to answer research questions and to annotate our pseudogenes appropriately. Finally, we were left with a knowledge base which could be queried to discover information about human pseudogene evolution.
引用
收藏
页码:i71 / i78
页数:8
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