rSW-seq is a tool to detect copy number variation (CNV). The rSW-seq method uses the Smith-Waterman local alignment algorithm with single-end sequencing data as the basis. The tool is available from the Authors upon request.
Genetics; Oncology; genetic variation
Kim TM, Luquette LJ, Xi R, Park PJ "rSW-seq: algorithm for detection of copy number alterations in deep sequencing data." BMC Bioinformatics. 2010 Aug 18;11:432. https://doi.org/10.1186/1471-2105-11-432
PMID: 20718989
PMCID: PMC2939611
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