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WISARD, a Workbench for Integrated Superfast Association study with Related Data is a statistical analysis toolkit for the analysis of large-scale single nucleotide polymorphism (SNP), copy number variation (CNV), and next-generation sequencing (NGS) data. With WISARD you can analyze related and unrelated samples. The code is optimized for running in multi-core CPUs.




  • Operation: Analysis; statistical analysis
  • Software interface: Command-line user interface; web user interface
  • Language: C++
  • Operating system: Linux; Microsoft Windows; Solaris; FreeBSD
  • License: Not stated
  • Cost: Free
  • Version name: 1.3.2
  • Credit: Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (HI16C2037). This work was supported by the Bio-Synergy Research Project (2013M3A9C4078158, NRF-2017M3A9C4065964) of the Ministry of Science, ICT and Future Planning through the National Research Foundation. The Boston EOCOPD Study was supported by NIH R01 HL113264. The Bio-Synergy Research Project (2013M3A9C4078158).
  • Contact: biznok _at_
  • Collection: -


Lee S, Choi S, Qiao D, Cho M, Silverman EK, Park T, Won S "WISARD: workbench for integrated superfast association studies for related datasets." BMC Med Genomics. 2018 Apr 20;11(Suppl 2):39.
PMID: 29697360
PMCID: PMC5918457

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