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Systematic errors in annotations of truncations, loss-of-function and synonymous variants

Description of genetic phenomena and variations requires exact language and concepts. Vast amounts of variation data are produced with next-generation sequencing pipelines. The obtained variations are automatically annotated, e.g., for their functional consequences. These tools and pipelines, along...

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Autor principal: Vihinen, Mauno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880313/
https://www.ncbi.nlm.nih.gov/pubmed/36713076
http://dx.doi.org/10.3389/fgene.2023.1015017
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author Vihinen, Mauno
author_facet Vihinen, Mauno
author_sort Vihinen, Mauno
collection PubMed
description Description of genetic phenomena and variations requires exact language and concepts. Vast amounts of variation data are produced with next-generation sequencing pipelines. The obtained variations are automatically annotated, e.g., for their functional consequences. These tools and pipelines, along with systematic nomenclature, mainly work well, but there are still some problems in nomenclature, organization of some databases, misuse of concepts and certain practices. Therefore, systematic errors prevent correct annotation and often preclude further analysis of certain variation types. Problems and solutions are described for presumed protein truncations, variants that are claimed to be of loss-of-function based on the type of variation, and synonymous variants that are not synonymous and lead to sequence changes or to missing protein.
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spelling pubmed-98803132023-01-28 Systematic errors in annotations of truncations, loss-of-function and synonymous variants Vihinen, Mauno Front Genet Genetics Description of genetic phenomena and variations requires exact language and concepts. Vast amounts of variation data are produced with next-generation sequencing pipelines. The obtained variations are automatically annotated, e.g., for their functional consequences. These tools and pipelines, along with systematic nomenclature, mainly work well, but there are still some problems in nomenclature, organization of some databases, misuse of concepts and certain practices. Therefore, systematic errors prevent correct annotation and often preclude further analysis of certain variation types. Problems and solutions are described for presumed protein truncations, variants that are claimed to be of loss-of-function based on the type of variation, and synonymous variants that are not synonymous and lead to sequence changes or to missing protein. Frontiers Media S.A. 2023-01-13 /pmc/articles/PMC9880313/ /pubmed/36713076 http://dx.doi.org/10.3389/fgene.2023.1015017 Text en Copyright © 2023 Vihinen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Vihinen, Mauno
Systematic errors in annotations of truncations, loss-of-function and synonymous variants
title Systematic errors in annotations of truncations, loss-of-function and synonymous variants
title_full Systematic errors in annotations of truncations, loss-of-function and synonymous variants
title_fullStr Systematic errors in annotations of truncations, loss-of-function and synonymous variants
title_full_unstemmed Systematic errors in annotations of truncations, loss-of-function and synonymous variants
title_short Systematic errors in annotations of truncations, loss-of-function and synonymous variants
title_sort systematic errors in annotations of truncations, loss-of-function and synonymous variants
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880313/
https://www.ncbi.nlm.nih.gov/pubmed/36713076
http://dx.doi.org/10.3389/fgene.2023.1015017
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