URL: https://github.com/PapenfussLab/gridss
Proper Citation: GRIDSS (RRID:SCR_027130)
Description: Software suite containing tools for detection of genomic rearrangements. Multithreaded structural variant (SV) caller that performs efficient genome-wide break-end assembly prior to variant calling using novel positional de Bruijn graph-based assembler. GRIDSS2 is structural variant caller to explicitly report single breakends-breakpoints in which only one side can be unambiguously determined.
Synonyms: GRIDSS2, Genomic Rearrangement IDentification Software Suite
Resource Type: software resource, software toolkit, source code
Defining Citation: PMID:29097403, PMID:34253237
Keywords: multithreaded structural variant caller, variant calling, detection of genomic rearrangements, structural variant caller, report single breakends-breakpoints,
Funding: Australian National Health and Medical Research Council
Availability: Free, Available for download, Freely available,
Resource Name: GRIDSS
Resource ID: SCR_027130
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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
