MBISON: Finding miRNA target over-representation in gene lists from ChIP-sequencing data

被引:2
|
作者
Gebhardt M.L. [1 ]
Mer A.S. [1 ,4 ]
Andrade-Navarro M.A. [1 ,2 ,3 ]
机构
[1] Max Delbrück Center for Molecular Medicine, Berlin
[2] Institute of Molecular Biology, Mainz
[3] Faculty of Biology, Johannes-Gutenberg University of Mainz, Mainz
[4] Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm
关键词
ChIP-sequencing; Data integration; Enrichment; Gene regulatory networks; microRNA; Target genes; Transcription factors;
D O I
10.1186/s13104-015-1118-8
中图分类号
学科分类号
摘要
Background: Over-representation of predicted miRNA targets in sets of genes regulated by a given transcription factor (e.g. as defined by ChIP-sequencing experiments) helps to identify biologically relevant miRNA targets and is useful to get insight into post-transcriptional regulation. Findings: To facilitate the application of this approach we have created the mBISON web-application. mBISON calculates the significance of over-representation of miRNA targets in a given non-ranked gene set. The gene set can be specified either by a list of genes or by one or more ChIP-seq datasets followed by a user-defined peak-gene association procedure. mBISON is based on predictions from TargetScan and uses a randomization step to calculate False-Discovery-Rates for each miRNA, including a correction for gene set specific properties such as 3'UTR length. The tool can be accessed from the following web-resource: http://cbdm.mdc-berlin.de/~mgebhardt/cgi-bin/mbison/home. Conclusion: mBISON is a web-application that helps to extract functional information about miRNAs from gene lists, which is in contrast to comparable applications easy to use by everyone and can be applied on ChIP-seq data directly. © 2015 Gebhardt et al.; licensee BioMed Central.
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