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URL: https://github.com/czc/nb_distribution
Proper Citation: NovoBreak (RRID:SCR_026032)
Description: Software tool to discover somatic and germline structural variation breakpoints in whole genome sequencing data. Can report accurate breakpoints of Deletions, Duplications, Inversions and Translocations. Designed for Illumina paired-end data. Local assembly for breakpoint detection in cancer genomes.
Resource Type: software application, software resource, source code
Defining Citation: PMID:27892959
Keywords: discover somatic and germline structural variation, structural variation breakpoints, whole-genome sequencing data, local assembly, breakpoint detection, cancer genomes,
Funding: NCI P30 CA016672; NCI R01 CA172652; NHGRI U41 HG007497
Availability: Free, Available for download, Freely available,
Resource Name: NovoBreak
Resource ID: SCR_026032
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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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