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InvFEST, a database integrating information of polymorphic inversions in the human genome
The newest genomic advances have uncovered an unprecedented degree of structural variation throughout genomes, with great amounts of data accumulating rapidly. Here we introduce InvFEST (http://invfestdb.uab.cat), a database combining multiple sources of information to generate a complete catalogue...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965118/ https://www.ncbi.nlm.nih.gov/pubmed/24253300 http://dx.doi.org/10.1093/nar/gkt1122 |
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author | Martínez-Fundichely, Alexander Casillas, Sònia Egea, Raquel Ràmia, Miquel Barbadilla, Antonio Pantano, Lorena Puig, Marta Cáceres, Mario |
author_facet | Martínez-Fundichely, Alexander Casillas, Sònia Egea, Raquel Ràmia, Miquel Barbadilla, Antonio Pantano, Lorena Puig, Marta Cáceres, Mario |
author_sort | Martínez-Fundichely, Alexander |
collection | PubMed |
description | The newest genomic advances have uncovered an unprecedented degree of structural variation throughout genomes, with great amounts of data accumulating rapidly. Here we introduce InvFEST (http://invfestdb.uab.cat), a database combining multiple sources of information to generate a complete catalogue of non-redundant human polymorphic inversions. Due to the complexity of this type of changes and the underlying high false-positive discovery rate, it is necessary to integrate all the available data to get a reliable estimate of the real number of inversions. InvFEST automatically merges predictions into different inversions, refines the breakpoint locations, and finds associations with genes and segmental duplications. In addition, it includes data on experimental validation, population frequency, functional effects and evolutionary history. All this information is readily accessible through a complete and user-friendly web report for each inversion. In its current version, InvFEST combines information from 34 different studies and contains 1092 candidate inversions, which are categorized based on internal scores and manual curation. Therefore, InvFEST aims to represent the most reliable set of human inversions and become a central repository to share information, guide future studies and contribute to the analysis of the functional and evolutionary impact of inversions on the human genome. |
format | Online Article Text |
id | pubmed-3965118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39651182014-03-25 InvFEST, a database integrating information of polymorphic inversions in the human genome Martínez-Fundichely, Alexander Casillas, Sònia Egea, Raquel Ràmia, Miquel Barbadilla, Antonio Pantano, Lorena Puig, Marta Cáceres, Mario Nucleic Acids Res VI. Genomic variation, diseases and drugs The newest genomic advances have uncovered an unprecedented degree of structural variation throughout genomes, with great amounts of data accumulating rapidly. Here we introduce InvFEST (http://invfestdb.uab.cat), a database combining multiple sources of information to generate a complete catalogue of non-redundant human polymorphic inversions. Due to the complexity of this type of changes and the underlying high false-positive discovery rate, it is necessary to integrate all the available data to get a reliable estimate of the real number of inversions. InvFEST automatically merges predictions into different inversions, refines the breakpoint locations, and finds associations with genes and segmental duplications. In addition, it includes data on experimental validation, population frequency, functional effects and evolutionary history. All this information is readily accessible through a complete and user-friendly web report for each inversion. In its current version, InvFEST combines information from 34 different studies and contains 1092 candidate inversions, which are categorized based on internal scores and manual curation. Therefore, InvFEST aims to represent the most reliable set of human inversions and become a central repository to share information, guide future studies and contribute to the analysis of the functional and evolutionary impact of inversions on the human genome. Oxford University Press 2014-01-01 2013-11-16 /pmc/articles/PMC3965118/ /pubmed/24253300 http://dx.doi.org/10.1093/nar/gkt1122 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 Martínez-Fundichely, Alexander Casillas, Sònia Egea, Raquel Ràmia, Miquel Barbadilla, Antonio Pantano, Lorena Puig, Marta Cáceres, Mario InvFEST, a database integrating information of polymorphic inversions in the human genome |
title | InvFEST, a database integrating information of polymorphic inversions in the human genome |
title_full | InvFEST, a database integrating information of polymorphic inversions in the human genome |
title_fullStr | InvFEST, a database integrating information of polymorphic inversions in the human genome |
title_full_unstemmed | InvFEST, a database integrating information of polymorphic inversions in the human genome |
title_short | InvFEST, a database integrating information of polymorphic inversions in the human genome |
title_sort | invfest, a database integrating information of polymorphic inversions in the human genome |
topic | VI. Genomic variation, diseases and drugs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965118/ https://www.ncbi.nlm.nih.gov/pubmed/24253300 http://dx.doi.org/10.1093/nar/gkt1122 |
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