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URL: https://github.com/NCI-CGR/PLP_prediction_workflow/tree/autogvp
Proper Citation: AutoGVP (RRID:SCR_026107)
Description: Software tool integrates ClinVar variant annotation with modified InterVar classification approach, based on American College of Medical Genetics-Association for Molecular Pathology guidelines, to output germline variant classification. Since AutoGVP input only requires VCF file, it can facilitate large-scale, clinically focused classification of germline sequence variants.
Synonyms: Automated Germline Variant Pathogenicity
Resource Type: software application, software resource, source code
Defining Citation: PMID:38426335
Keywords: germline variant classification, germline sequence variants, germline, sequence variants,
Funding: NCI R01CA237562; NCI R03CA230366; NCI R03CA287169
Availability: Free, Available for download, Freely available
Resource Name: AutoGVP
Resource ID: SCR_026107
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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
The data sets included in this resource are published in Kravitz et al, 2012. Distinct roles for direct and indirect pathway striatal neurons in reinforcement (Nat. Neurosci).
