JointSLM an R package for the detection of copy number variation (CNV). The algorithm analyses coverage data simultaneously within multiple samples.
DNA structural variation
Magi A, Benelli M, Yoon S, Roviello F, Torricelli F "Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm." Nucleic Acids Res. 2011 May;39(10):e65. https://doi.org/10.1093/nar/gkr068
PMID: 21321017
PMCID: PMC3105418
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