Show simple item record

dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMEGUERDITCHIAN, Caroline
dc.contributor.authorBAUX, David
dc.contributor.authorLUDWIG, Thomas E
dc.contributor.authorGENIN, Emmanuelle
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorTREGOUET, David-Alexandre
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorSOUKARIEH, Omar
dc.date.accessioned2025-04-23T09:52:22Z
dc.date.available2025-04-23T09:52:22Z
dc.date.issued2025-03-01
dc.identifier.issn2631-9268en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/206359
dc.description.abstractEnNon-canonical small open reading frames (sORFs) are among the main regulators of gene expression. The most studied of these are upstream ORFs (upORFs) located in the 5,-untranslated region (UTR) of coding genes. Internal ORFs (intORFs) in the coding sequence and downstream ORFs (dORFs) in the 3,UTR have received less attention. Different bioinformatics tools permit the prediction of single nucleotide variants (SNVs) altering upORFs, mainly those creating AUGs or deleting stop codons, but no tool predicts variants altering non-canonical translation initiation sites and those altering intORFs or dORFs. We propose an upgrade of our MORFEE bioinformatics tool to identify SNVs that may alter all types of sORFs in coding transcripts from a VCF file. Moreover, we generate an exhaustive catalog, named MORFEEdb, reporting all possible SNVs altering existing upORFs or creating new ones in human transcripts, and provide an R script for visualizing the results. MORFEEdb has been implemented in the public platform Mobidetails. Finally, the annotation of ClinVar variants with MORFEE reveals that > 45% of UTR-SNVs can alter upORFs or dORFs. In conclusion, MORFEE and MORFEEdb have the potential to improve the molecular diagnosis of rare human diseases and to facilitate the identification of functional variants from genome-wide association studies of complex traits. © The Author(s) 2025.
dc.description.sponsorshipEtude du caractère pathogène de variants créant des cadres de lecture ouverts en amont de la séquence codante de l'endogline - Nouvelles perspectives thérapeutiques pour la maladie du Rendu-Osler - ANR-23-CE17-0042en_US
dc.description.sponsorshipVaincre les maladies vasculaires cérébrales par un nouveau paradigme de prévention de précision et d'innovation thérapeutique - ANR-23-IAHU-0001en_US
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.title.enEnhancing the annotation of small ORF-altering variants using MORFEE: introducing MORFEEdb, a comprehensive catalog of SNVs affecting upstream ORFs in human 5,UTRs
dc.title.alternativeNAR Genom Bioinformen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/nargab/lqaf017
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed40109352en_US
bordeaux.journalNAR Genomics and Bioinformaticsen_US
bordeaux.pagelqaf017en_US
bordeaux.volume7en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamELEANOR_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.description.error
hal.identifierhal-05043945
hal.version1
hal.date.transferred2025-04-23T10:23:43Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.update-error.statusmetadataUpdate
hal.update-error.statusmetadataUpdate
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=NAR%20Genomics%20and%20Bioinformatics&rft.date=2025-03-01&rft.volume=7&rft.issue=1&rft.spage=lqaf017&rft.epage=lqaf017&rft.eissn=2631-9268&rft.issn=2631-9268&rft.au=MEGUERDITCHIAN,%20Caroline&BAUX,%20David&LUDWIG,%20Thomas%20E&GENIN,%20Emmanuelle&TREGOUET,%20David-Alexandre&rft.genre=article


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record