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URL: https://code.google.com/p/nfuse/
Proper Citation: nFuse (RRID:SCR_000066)
Description: Software that predicts fusion transcripts and associated CGRs from matched RNA-seq and Whole Genome Shotgun Sequencing (WGSS).
Abbreviations: nFuse
Synonyms: nFuse: Discovery of Complex Genomic Rearrangements in Cancer
Resource Type: software resource
Defining Citation: PMID:22745232
Keywords: cancer, genomics
Related Condition: Cancer
Availability: Free, Available for download, Freely available,
Resource Name: nFuse
Resource ID: SCR_000066
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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