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URL: https://github.com/cc2qe/speedseq
Proper Citation: SpeedSeq (RRID:SCR_000469)
Description: Software for a lightweight, flexible, and open source pipeline that identifies genomic variation (single nucleotide variants (SNVs), indels, and structural variants (SVs)).
Resource Type: software resource
Keywords: standalone software
Availability: Free, Available for download, Freely available
Resource Name: SpeedSeq
Resource ID: SCR_000469
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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
