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URL: https://github.com/BGI-Qingdao/TGS-GapCloser
Proper Citation: TGS-GapCloser (RRID:SCR_017633)
Description: Software tool that uses long reads to enhance genome assembly. Fast and accurate gap closing software tool that uses low coverage of error-prone long reads generated by third generation sequence techniques (Pacbio, Oxford Nanopore, etc.) or preassembled contigs for large genomes.
Resource Type: data processing software, software application, software resource
Keywords: Error, prone, third, generation, sequencing, long, read, gap, closing, genome, assembly, contig, bio.tools
Availability: Free, Available for download, Freely available
Resource Name: TGS-GapCloser
Resource ID: SCR_017633
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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
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