URL: https://github.com/AIRI-Institute/DeepCT
Proper Citation: DeepCT (RRID:SCR_023302)
Description: Software tool can learn complex interconnections of epigenetic features and infer unmeasured data from any available input. Can learn cell type-specific properties, build biologically meaningful vector representations of cell types, and utilize these representations to generate cell type-specific predictions of effects of non-coding variations in human genome.
Resource Type: data analysis software, data processing software, software application, software resource
Defining Citation: DOI:10.1101/2021.12.31.474623
Keywords: interconnections of epigenetic features, infer unmeasured data, human genome
Availability: Free, Available for download, Freely available
Resource Name: DeepCT
Resource ID: SCR_023302
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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
