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.
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. https://doi.org/10.1186/s12920-018-0345-y
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