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URL: https://github.com/PedroBarbosa/DeepIntronic_Benchmark
Proper Citation: Benchmark of human deep intronic variation (RRID:SCR_023315)
Description: Repository of code, data, and documentation to reproduce computational evaluation performed to identify the best tools/models to predict genetic variation in deep intronic regions of human genome.
Synonyms: Benchmark of deep intronic variation
Resource Type: software resource
Defining Citation: DOI:10.1101/2023.02.17.528928
Keywords: reproduce computational evaluation, predict genetic variation, deep intronic regions, human genome
Availability: Free, Available for download, Freely available
Resource Name: Benchmark of human deep intronic variation
Resource ID: SCR_023315
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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