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Mutalyzer 2: next generation HGVS nomenclature checker
MOTIVATION: Unambiguous variant descriptions are of utmost importance in clinical genetic diagnostics, scientific literature and genetic databases. The Human Genome Variation Society (HGVS) publishes a comprehensive set of guidelines on how variants should be correctly and unambiguously described. W...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479679/ https://www.ncbi.nlm.nih.gov/pubmed/33538839 http://dx.doi.org/10.1093/bioinformatics/btab051 |
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author | Lefter, Mihai Vis, Jonathan K Vermaat, Martijn den Dunnen, Johan T Taschner, Peter E M Laros, Jeroen F J |
author_facet | Lefter, Mihai Vis, Jonathan K Vermaat, Martijn den Dunnen, Johan T Taschner, Peter E M Laros, Jeroen F J |
author_sort | Lefter, Mihai |
collection | PubMed |
description | MOTIVATION: Unambiguous variant descriptions are of utmost importance in clinical genetic diagnostics, scientific literature and genetic databases. The Human Genome Variation Society (HGVS) publishes a comprehensive set of guidelines on how variants should be correctly and unambiguously described. We present the implementation of the Mutalyzer 2 tool suite, designed to automatically apply the HGVS guidelines so users do not have to deal with the HGVS intricacies explicitly to check and correct their variant descriptions. RESULTS: Mutalyzer is profusely used by the community, having processed over 133 million descriptions since its launch. Over a five year period, Mutalyzer reported a correct input in ∼50% of cases. In 41% of the cases either a syntactic or semantic error was identified and for ∼7% of cases, Mutalyzer was able to automatically correct the description. AVAILABILITY AND IMPLEMENTATION: Mutalyzer is an Open Source project under the GNU Affero General Public License. The source code is available on GitHub (https://github.com/mutalyzer/mutalyzer) and a running instance is available at: https://mutalyzer.nl |
format | Online Article Text |
id | pubmed-8479679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84796792021-09-30 Mutalyzer 2: next generation HGVS nomenclature checker Lefter, Mihai Vis, Jonathan K Vermaat, Martijn den Dunnen, Johan T Taschner, Peter E M Laros, Jeroen F J Bioinformatics Original Papers MOTIVATION: Unambiguous variant descriptions are of utmost importance in clinical genetic diagnostics, scientific literature and genetic databases. The Human Genome Variation Society (HGVS) publishes a comprehensive set of guidelines on how variants should be correctly and unambiguously described. We present the implementation of the Mutalyzer 2 tool suite, designed to automatically apply the HGVS guidelines so users do not have to deal with the HGVS intricacies explicitly to check and correct their variant descriptions. RESULTS: Mutalyzer is profusely used by the community, having processed over 133 million descriptions since its launch. Over a five year period, Mutalyzer reported a correct input in ∼50% of cases. In 41% of the cases either a syntactic or semantic error was identified and for ∼7% of cases, Mutalyzer was able to automatically correct the description. AVAILABILITY AND IMPLEMENTATION: Mutalyzer is an Open Source project under the GNU Affero General Public License. The source code is available on GitHub (https://github.com/mutalyzer/mutalyzer) and a running instance is available at: https://mutalyzer.nl Oxford University Press 2021-02-04 /pmc/articles/PMC8479679/ /pubmed/33538839 http://dx.doi.org/10.1093/bioinformatics/btab051 Text en © The Author(s) 2021. 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 | Original Papers Lefter, Mihai Vis, Jonathan K Vermaat, Martijn den Dunnen, Johan T Taschner, Peter E M Laros, Jeroen F J Mutalyzer 2: next generation HGVS nomenclature checker |
title | Mutalyzer 2: next generation HGVS nomenclature checker |
title_full | Mutalyzer 2: next generation HGVS nomenclature checker |
title_fullStr | Mutalyzer 2: next generation HGVS nomenclature checker |
title_full_unstemmed | Mutalyzer 2: next generation HGVS nomenclature checker |
title_short | Mutalyzer 2: next generation HGVS nomenclature checker |
title_sort | mutalyzer 2: next generation hgvs nomenclature checker |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8479679/ https://www.ncbi.nlm.nih.gov/pubmed/33538839 http://dx.doi.org/10.1093/bioinformatics/btab051 |
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