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RevUP: an online scoring system for regulatory variants implicated in rare diseases
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 va...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048665/ https://www.ncbi.nlm.nih.gov/pubmed/35289834 http://dx.doi.org/10.1093/bioinformatics/btac157 |
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author | Correard, Solenne Hewitson, Brittany van der Lee, Robin Wasserman, Wyeth W |
author_facet | Correard, Solenne Hewitson, Brittany van der Lee, Robin Wasserman, Wyeth W |
author_sort | Correard, Solenne |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9048665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-90486652022-04-29 RevUP: an online scoring system for regulatory variants implicated in rare diseases Correard, Solenne Hewitson, Brittany van der Lee, Robin Wasserman, Wyeth W Bioinformatics Applications Notes 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. Oxford University Press 2022-03-15 /pmc/articles/PMC9048665/ /pubmed/35289834 http://dx.doi.org/10.1093/bioinformatics/btac157 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Applications Notes Correard, Solenne Hewitson, Brittany van der Lee, Robin Wasserman, Wyeth W RevUP: an online scoring system for regulatory variants implicated in rare diseases |
title | RevUP: an online scoring system for regulatory variants implicated in rare diseases |
title_full | RevUP: an online scoring system for regulatory variants implicated in rare diseases |
title_fullStr | RevUP: an online scoring system for regulatory variants implicated in rare diseases |
title_full_unstemmed | RevUP: an online scoring system for regulatory variants implicated in rare diseases |
title_short | RevUP: an online scoring system for regulatory variants implicated in rare diseases |
title_sort | revup: an online scoring system for regulatory variants implicated in rare diseases |
topic | Applications Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9048665/ https://www.ncbi.nlm.nih.gov/pubmed/35289834 http://dx.doi.org/10.1093/bioinformatics/btac157 |
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