For better experience, turn on JavaScript!



JointSLM an R package for the detection of copy number variation (CNV). The algorithm analyses coverage data simultaneously within multiple samples.


DNA structural variation


  • Operation: Genetic variation analysis
  • Software interface: Command-line user interface; Library
  • Language: R
  • Operating system: Linux; Mac OS X; Microsoft Windows
  • License: Not stated
  • Cost: Free
  • Version name: -
  • Credit: The Istituto Toscano Tumori (ITT).
  • Contact: Alberto Magi albertomagi _at_
  • Collection: -


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.
PMID: 21321017
PMCID: PMC3105418

Download and documentation

If you find errors, please report here.