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NECTAR: a database of codon-centric missense variant annotations

NECTAR (Non-synonymous Enriched Coding muTation ARchive; http://nectarmutation.org) is a database and web application to annotate disease-related and functionally important amino acids in human proteins. A number of tools are available to facilitate the interpretation of DNA variants identified in d...

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Autores principales: Gong, Sungsam, Ware, James S., Walsh, Roddy, Cook, Stuart A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965063/
https://www.ncbi.nlm.nih.gov/pubmed/24297257
http://dx.doi.org/10.1093/nar/gkt1245
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author Gong, Sungsam
Ware, James S.
Walsh, Roddy
Cook, Stuart A.
author_facet Gong, Sungsam
Ware, James S.
Walsh, Roddy
Cook, Stuart A.
author_sort Gong, Sungsam
collection PubMed
description NECTAR (Non-synonymous Enriched Coding muTation ARchive; http://nectarmutation.org) is a database and web application to annotate disease-related and functionally important amino acids in human proteins. A number of tools are available to facilitate the interpretation of DNA variants identified in diagnostic or research sequencing. These typically identify previous reports of DNA variation at a given genomic location, predict its effects on transcript and protein sequence and may predict downstream functional consequences. Previous reports and functional annotations are typically linked by the genomic location of the variant observed. NECTAR collates disease-causing variants and functionally important amino acid residues from a number of sources. Importantly, rather than simply linking annotations by a shared genomic location, NECTAR annotates variants of interest with details of previously reported variation affecting the same codon. This provides a much richer data set for the interpretation of a novel DNA variant. NECTAR also identifies functionally equivalent amino acid residues in evolutionarily related proteins (paralogues) and, where appropriate, transfers annotations between them. As well as accessing these data through a web interface, users can upload batches of variants in variant call format (VCF) for annotation on-the-fly. The database is freely available to download from the ftp site: ftp://ftp.nectarmutation.org.
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spelling pubmed-39650632014-03-25 NECTAR: a database of codon-centric missense variant annotations Gong, Sungsam Ware, James S. Walsh, Roddy Cook, Stuart A. Nucleic Acids Res VI. Genomic variation, diseases and drugs NECTAR (Non-synonymous Enriched Coding muTation ARchive; http://nectarmutation.org) is a database and web application to annotate disease-related and functionally important amino acids in human proteins. A number of tools are available to facilitate the interpretation of DNA variants identified in diagnostic or research sequencing. These typically identify previous reports of DNA variation at a given genomic location, predict its effects on transcript and protein sequence and may predict downstream functional consequences. Previous reports and functional annotations are typically linked by the genomic location of the variant observed. NECTAR collates disease-causing variants and functionally important amino acid residues from a number of sources. Importantly, rather than simply linking annotations by a shared genomic location, NECTAR annotates variants of interest with details of previously reported variation affecting the same codon. This provides a much richer data set for the interpretation of a novel DNA variant. NECTAR also identifies functionally equivalent amino acid residues in evolutionarily related proteins (paralogues) and, where appropriate, transfers annotations between them. As well as accessing these data through a web interface, users can upload batches of variants in variant call format (VCF) for annotation on-the-fly. The database is freely available to download from the ftp site: ftp://ftp.nectarmutation.org. Oxford University Press 2014-01-01 2013-11-30 /pmc/articles/PMC3965063/ /pubmed/24297257 http://dx.doi.org/10.1093/nar/gkt1245 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle VI. Genomic variation, diseases and drugs
Gong, Sungsam
Ware, James S.
Walsh, Roddy
Cook, Stuart A.
NECTAR: a database of codon-centric missense variant annotations
title NECTAR: a database of codon-centric missense variant annotations
title_full NECTAR: a database of codon-centric missense variant annotations
title_fullStr NECTAR: a database of codon-centric missense variant annotations
title_full_unstemmed NECTAR: a database of codon-centric missense variant annotations
title_short NECTAR: a database of codon-centric missense variant annotations
title_sort nectar: a database of codon-centric missense variant annotations
topic VI. Genomic variation, diseases and drugs
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965063/
https://www.ncbi.nlm.nih.gov/pubmed/24297257
http://dx.doi.org/10.1093/nar/gkt1245
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