TAM: A method for enrichment and depletion analysis of a microRNA category in a list of microRNAs

被引:120
作者
Lu, Ming [1 ]
Shi, Bing [1 ,2 ]
Wang, Juan [1 ]
Cao, Qun [1 ]
Cui, Qinghua [1 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Dept Biomed Informat, Beijing 100191, Peoples R China
[2] Beijing Mil Gen Hosp, Dept Cardiol, Beijing 100700, Peoples R China
来源
BMC BIOINFORMATICS | 2010年 / 11卷
关键词
TARGET; REVEALS;
D O I
10.1186/1471-2105-11-419
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: MicroRNAs (miRNAs) are a class of important gene regulators. The number of identified miRNAs has been increasing dramatically in recent years. An emerging major challenge is the interpretation of the genome-scale miRNA datasets, including those derived from microarray and deep-sequencing. It is interesting and important to know the common rules or patterns behind a list of miRNAs, (i.e. the deregulated miRNAs resulted from an experiment of miRNA microarray or deep-sequencing). Results: For the above purpose, this study presents a method and develops a tool (TAM) for annotations of meaningful human miRNAs categories. We first integrated miRNAs into various meaningful categories according to prior knowledge, such as miRNA family, miRNA cluster, miRNA function, miRNA associated diseases, and tissue specificity. Using TAM, given lists of miRNAs can be rapidly annotated and summarized according to the integrated miRNA categorical data. Moreover, given a list of miRNAs, TAM can be used to predict novel related miRNAs. Finally, we confirmed the usefulness and reliability of TAM by applying it to deregulated miRNAs in acute myocardial infarction (AMI) from two independent experiments. Conclusion: TAM can efficiently identify meaningful categories for given miRNAs. In addition, TAM can be used to identify novel miRNA biomarkers. TAM tool, source codes, and miRNA category data are freely available at http://cmbi.bjmu.edu.cn/tam.
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页数:7
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