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dc.rights.licenseopenen_US
dc.contributor.authorASGARI, Yazdan
dc.contributor.authorSUGIER, Pierre-Emmanuel
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBAGHFALAKI, Taban
dc.contributor.authorLUCOTTE, Elise
dc.contributor.authorKARIMI, Mojgan
dc.contributor.authorSEDKI, Mohammed
dc.contributor.authorNGO, Amélie
dc.contributor.authorLIQUET, Benoit
dc.contributor.authorTRUONG, Thérèse
dc.date.accessioned2023-11-07T14:01:53Z
dc.date.available2023-11-07T14:01:53Z
dc.date.issued2023-09-01
dc.identifier.issn2631-9268en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184659
dc.description.abstractEnCross-phenotype association using gene-set analysis can help to detect pleiotropic genes and inform about common mechanisms between diseases. Although there are an increasing number of statistical methods for exploring pleiotropy, there is a lack of proper pipelines to apply gene-set analysis in this context and using genome-scale data in a reasonable running time. We designed a user-friendly pipeline to perform cross-phenotype gene-set analysis between two traits using GCPBayes, a method developed by our team. All analyses could be performed automatically by calling for different scripts in a simple way (using a Shiny app, Bash or R script). A Shiny application was also developed to create different plots to visualize outputs from GCPBayes. Finally, a comprehensive and step-by-step tutorial on how to use the pipeline is provided in our group's GitHub page. We illustrated the application on publicly available GWAS (genome-wide association studies) summary statistics data to identify breast cancer and ovarian cancer susceptibility genes. We have shown that the GCPBayes pipeline could extract pleiotropic genes previously mentioned in the literature, while it also provided new pleiotropic genes and regions that are worthwhile for further investigation. We have also provided some recommendations about parameter selection for decreasing computational time of GCPBayes on genome-scale data.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.title.enGCPBayes pipeline: a tool for exploring pleiotropy at the gene level
dc.title.alternativeNAR Genom Bioinformen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/nargab/lqad065en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed37416786en_US
dc.description.sponsorshipEuropeEuropean Union’s Horizon 2020 research and innovation programmeen_US
bordeaux.journalNAR Genomics and Bioinformaticsen_US
bordeaux.pagelqad065en_US
bordeaux.volume5en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamBIOSTATen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDLigue Contre le Canceren_US
bordeaux.import.sourcepubmed
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcepubmed
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=2023-09-01&rft.volume=5&rft.issue=3&rft.spage=lqad065&rft.epage=lqad065&rft.eissn=2631-9268&rft.issn=2631-9268&rft.au=ASGARI,%20Yazdan&SUGIER,%20Pierre-Emmanuel&BAGHFALAKI,%20Taban&LUCOTTE,%20Elise&KARIMI,%20Mojgan&rft.genre=article


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