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URL: https://github.com/brentp/duphold
Proper Citation: duphold (RRID:SCR_016938)
Description: Software tool to annotate structural variant calls with sequence depth information that can add or remove confidence to SV predicted to affect copy number. Indicates the presence of a rapid change in depth relative to the regions surrounding the breakpoints. Allows the run time to be nearly independent of the number of variants important for large, jointly called projects with many samples. Annotates structural variant predictions made from both short read and long read data.
Resource Type: data analysis software, data processing software, software application, software resource
Keywords: annotate, structural, variation, call, sequence, depth, confidence, predict, copy, number, short, long, read, data
Availability: Free, Available for download, Freely available
Resource Name: duphold
Resource ID: SCR_016938
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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