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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.
Afiliação
  • Lefter M; Department of Human Genetics, Leiden University Medical Center (LUMC)Leiden, The Netherlands.
  • Vis JK; Department of Human Genetics, Leiden University Medical Center (LUMC)Leiden, The Netherlands.
  • Vermaat M; Department of Clinical Genetics, Leiden University Medical Center (LUMC)Leiden, The Netherlands.
  • den Dunnen JT; Department of Human Genetics, Leiden University Medical Center (LUMC)Leiden, The Netherlands.
  • Taschner PEM; Department of Human Genetics, Leiden University Medical Center (LUMC)Leiden, The Netherlands.
  • Laros JFJ; Department of Clinical Genetics, Leiden University Medical Center (LUMC)Leiden, The Netherlands.
Bioinformatics ; 37(18): 2811-2817, 2021 09 29.
Article em En | MEDLINE | ID: mdl-33538839
ABSTRACT
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Software Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Software Idioma: En Ano de publicação: 2021 Tipo de documento: Article