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Structural genomic variations play an important role in human disease and phenotypic diversity. With the rise of high-throughput sequencing tools, mate-pair/ paired-end/single-read sequencing has become an important technique for the detection and exploration of structural variation. Several analysis tools exist to handle different parts and aspects of such sequencing based structural variation analyses pipelines. A comprehensive analysis platform to handle all steps, from processing thedoi:10.1371/journal.pone.0113800 pmid:25503062 pmcid:PMC4264741 fatcat:uxfh3bzqwvbwlkhvulq6h6ty3i