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dc.rights.licenseopenen_US
hal.structure.identifierInstitut de biochimie et génétique cellulaires [IBGC]
dc.contributor.authorGALVIS, Johanna
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorGUYON, Joris
hal.structure.identifierCentre de Bioinformatique de Bordeaux [CBIB]
dc.contributor.authorDARTIGUES, Benjamin
dc.contributor.authorHECHT, Helge
dc.contributor.authorGRÜNING, Björn
hal.structure.identifierInstitut de biochimie et génétique cellulaires [IBGC]
dc.contributor.authorSPECQUE, Florian
dc.contributor.authorSOUEIDAN, Hayssam
hal.structure.identifierInstitut de biochimie et génétique cellulaires [IBGC]
dc.contributor.authorKARKAR, Slim
hal.structure.identifierInstitut de biochimie et génétique cellulaires [IBGC]
dc.contributor.authorDAUBON, Thomas
hal.structure.identifierInstitut de biochimie et génétique cellulaires [IBGC]
dc.contributor.authorNIKOLSKI, Macha
dc.date.accessioned2024-10-31T08:57:13Z
dc.date.available2024-10-31T08:57:13Z
dc.date.issued2024-05-02
dc.identifier.issn1367-4803en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203072
dc.description.abstractEnAbstract Motivation Many diseases, such as cancer, are characterized by an alteration of cellular metabolism allowing cells to adapt to changes in the microenvironment. Stable isotope-resolved metabolomics (SIRM) and downstream data analyses are widely used techniques for unraveling cells’ metabolic activity to understand the altered functioning of metabolic pathways in the diseased state. While a number of bioinformatic solutions exist for the differential analysis of SIRM data, there is currently no available resource providing a comprehensive toolbox. Results In this work, we present DIMet, a one-stop comprehensive tool for differential analysis of targeted tracer data. DIMet accepts metabolite total abundances, isotopologue contributions, and isotopic mean enrichment, and supports differential comparison (pairwise and multi-group), time-series analyses, and labeling profile comparison. Moreover, it integrates transcriptomics and targeted metabolomics data through network-based metabolograms. We illustrate the use of DIMet in real SIRM datasets obtained from Glioblastoma P3 cell-line samples. DIMet is open-source, and is readily available for routine downstream analysis of isotope-labeled targeted metabolomics data, as it can be used both in the command line interface or as a complete toolkit in the public Galaxy Europe and Workfow4Metabolomics web platforms. Availability and implementation DIMet is freely available at https://github.com/cbib/DIMet, and through https://usegalaxy.eu and https://workflow4metabolomics.usegalaxy.fr. All the datasets are available at Zenodo https://zenodo.org/records/10925786.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.title.enDIMet: an open-source tool for differential analysis of targeted isotope-labeled metabolomics data
dc.title.alternativeBioinformaticsen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/bioinformatics/btae282en_US
dc.subject.halSciences du Vivant [q-bio]en_US
dc.subject.halInformatique [cs]en_US
dc.identifier.pubmed38656970en_US
bordeaux.journalBioinformaticsen_US
bordeaux.pagebtae282en_US
bordeaux.volume40en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue5en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.institutionCNRS
bordeaux.teamAHEAD_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDInstitut National Du Canceren_US
bordeaux.identifier.funderIDHorizon 2020 Framework Programmeen_US
bordeaux.import.sourcehal
hal.identifierhal-04591269
hal.version1
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Bioinformatics&rft.date=2024-05-02&rft.volume=40&rft.issue=5&rft.spage=btae282&rft.epage=btae282&rft.eissn=1367-4803&rft.issn=1367-4803&rft.au=GALVIS,%20Johanna&GUYON,%20Joris&DARTIGUES,%20Benjamin&HECHT,%20Helge&GR%C3%9CNING,%20Bj%C3%B6rn&rft.genre=article


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