Abstract

BackgroundOver-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.FindingsTo 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.ConclusionmBISON 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.

Highlights

  • Over-representation of predicted miRNA targets in sets of genes regulated by a given transcription factor helps to identify biologically relevant miRNA targets and is useful to get insight into post-transcriptional regulation

  • It has been demonstrated that sets of functionally related genes, e.g. genes from a protein complex [1] or sets regulated by a common transcription factor [2,3], may contain information about their regulation on post-transcriptional level, which can be uncovered by means of enrichment analysis of miRNA targets

  • An application of such enrichment analysis can facilitate the classification of predicted miRNA targets according to their likelihood of being biologically functional and can point to miRNA function [2]

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Summary

Introduction

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. An application of such enrichment analysis can facilitate the classification of predicted miRNA targets according to their likelihood of being biologically functional and can point to miRNA function [2]. The mBISON (miRNA binding site over-representation) tool was developed to enable the direct use of gene lists or ChIP-seq data to address the above mentioned questions.

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Conclusion
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