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URL: http://sourceforge.net/projects/gmcloser/
Proper Citation: GMcloser (RRID:SCR_000646)
Description: Software that fills and closes the gaps present in scaffold assemblies, especially those generated by the de novo assembly of whole genomes with next-generation sequencing (NGS) reads. Unlike other gap-closing tools that use only NGS reads, GMcloser uses preassembled contig sets or long read sets as the sequences to close gaps and uses paired-end (PE) reads and a likelihood-based algorithm to improve the accuracy and efficiency of gap closure. The efficiency of gap closure can be increased by successive treatments with different contig sets.
Abbreviations: GMcloser
Synonyms: Gmcloser - Closing the gaps in scaffolds with preassembled contigs
Resource Type: software resource
Defining Citation: PMID:26261222
Keywords: scaffolding, bio.tools
Availability: Free, Available for download, Freely available
Resource Name: GMcloser
Resource ID: SCR_000646
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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