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URL: https://compbio.berkeley.edu/proj/strvctvre/
Proper Citation: StrVCTVRE (RRID:SCR_021776)
Description: Software tool as structural variant classifier for exonic deletions and duplications. Supervised learning method to predict pathogenicity of human genome structural variants.Used to distinguish pathogenic SVs from benign SVs that overlap exons.
Synonyms: Structural Variant Classifier Trained on Variants Rare and Exonic
Resource Type: data analysis software, data processing software, software resource, software application
Defining Citation: DOI:10.1101/2020.05.15.097048
Keywords: structural variant classifier, exonic deletions, human genome structural variants, predict pathogenicity, pathogenic SVs, benign SVs
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Source: SciCrunch Registry
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