Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Martínez-Fundichely, Alexander, Casillas, Sònia, Egea, Raquel, Ràmia, Miquel, Barbadilla, Antonio, Pantano, Lorena, Puig, Marta, Cáceres, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
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
_version_ 1782479302475907072
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
work_keys_str_mv AT martinezfundichelyalexander invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome
AT casillassonia invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome
AT egearaquel invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome
AT ramiamiquel invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome
AT barbadillaantonio invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome
AT pantanolorena invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome
AT puigmarta invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome
AT caceresmario invfestadatabaseintegratinginformationofpolymorphicinversionsinthehumangenome