BreakPtr, discovery of unbalanced structural variants (copy-number variants) with tiling microarrays
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BreakSeq, structural variant genotyping using split reads
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CopySeq, genotyping of unbalanced structural variants (copy-number variants) using read-depth
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DELLY, integrated split-read and paired-end based structural variant discovery in deep sequencing data
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PEMer, structural variant discovery in 454 sequencing data by paired-end mapping
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