<p><b>Step 1:</b> Four miRNAs known to be involved in prostate cancer <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0082160#pone.0082160-Heneghan1" target="_blank">[27]</a> are visualised in a Cytoscape network (A). The miRNAs are annotated with miRBase accession numbers and ids. <b>Step 2:</b> The regulatory interaction networks (RegINs) harbouring miRNA-target interactions (MTIs), either validated (miRecords and miRTarBase) or predicted (microCosm and TargetScan), are downloaded from <a href="http://projects.bigcat.unimaas.nl/cytargetlinker/regins" target="_blank">http://projects.bigcat.unimaas.nl/cytargetlinker/regins</a>. <b>Step 3:</b> Known targets are integrated (B) after specifying the miRBase accession number column, the RegINs directory and the direction “<i>Add Targets</i>” in the CyTargetLinker dialog. In the resulting network miRNAs and target genes are defined as grey circles and pink hexagons, respectively. The predicted MTIs are visualised in orange (TargetScan: 4239) and blue (microCosm: 2800) and the validated MTIs in red (miRTarBase: 59) and purple (miRecords: 24), as shown in the control panel. <b>Step 4:</b> The hide/show and overlap threshold functions were used to visualise validated interactions exclusively or to show the overlap in MTI coverage. In the validated network only the MTIs in miRecords and miRTarBase are visualised by hiding MTIs in TargetScan and microCosm (C). In the overlap network the MTIs present in two or more RegINs are shown by setting the threshold to 2 (D).</p
