URL: https://github.com/MHH-Bioinformatics-Hematology/vardictcpp
Proper Citation: vardictcpp (RRID:SCR_028800)
Description: Software tool as C++ implementation of the variant caller VarDict used in cancer research and clinical genomics to analyze next-generation sequencing (NGS) data from DNA or RNA samples to detect genetic mutations.
Resource Type: software application, software resource, source code
Keywords: Variant Calling, C++, VAF, analyze next-generation sequencing data, detect genetic mutations,
Availability: Free, Available for download, Freely available
Resource Name: vardictcpp
Resource ID: SCR_028800
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
