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URL: https://github.com/GATB/MindTheGap
Proper Citation: MindTheGap (RRID:SCR_024115)
Description: Software tool to perform detection and assembly of DNA insertion variants in NGS read datasets with respect to reference genome.Used to call insertions of any size, whether they are novel or duplicated, homozygous or heterozygous in the donor genome.
Synonyms: mindthegap
Resource Type: data analysis software, data processing software, software application, software resource
Keywords: perform detection and assembly of DNA insertion variants, NGS read datasets, reference genome, call insertions, donor genome,
Availability: Free, Available for download, Freely available,
Resource Name: MindTheGap
Resource ID: SCR_024115
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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
