Summary: To address the difficulty in assessing the implication of regulatory variants in diseases, a scoring scheme previously published allows the calculation of the Regulatory Variant Evidence score (RVE-score). The score represents the accumulated evidence for a causative role of a regulatory variant in a disease. Regulatory Evidence for Variants Underlying Phenotypes was built to calculate the RVE-score of regulatory variants, based on the 24 criteria, with a hybrid approach combining information retrieved from public databases and user input.
Availability And Implementation: RevUP is freely available at http://www.revup-classifier.ca. The source code is available at https://github.com/wassermanlab/revup.
Supplementary Information: Supplementary data are available at Bioinformatics online.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048665 | PMC |
http://dx.doi.org/10.1093/bioinformatics/btac157 | DOI Listing |
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