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URL: http://sourceforge.net/projects/mendelscan/
Proper Citation: MendelScan (RRID:SCR_013053)
Description: A software tool for prioritizing candidate variants in family-based studies of inherited disease.
Abbreviations: MendelScan
Synonyms: MendelScan - Variant scoring and linkage mapping for family exome sequencing
Resource Type: software resource
Keywords: matlab
Availability: GNU General Public License, v2
Resource Name: MendelScan
Resource ID: SCR_013053
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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
