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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: software resource, software application, data processing software, data analysis software
Keywords: perform detection and assembly of DNA insertion variants, NGS read datasets, reference genome, call insertions, donor genome,
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