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dc.rights.licenseopenen_US
hal.structure.identifierCentre de résonance magnétique des systèmes biologiques [CRMSB]
dc.contributor.authorBRINGAUD, Frederic
dc.contributor.authorROGERS, Matthew
dc.contributor.authorGHEDIN, Elodie
dc.date.accessioned2023-11-03T10:06:14Z
dc.date.available2023-11-03T10:06:14Z
dc.date.issued2015-01-01
dc.identifier.issn1940-6029en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184585
dc.description.abstractEnTransposable elements (TE), defined as discrete pieces of DNA that can move from one site to another site in genomes, represent significant components of eukaryotic genomes, including trypanosomatids. Up to 5% of the trypanosomatid genome content is composed of retroposons of the ingi clade, further divided into subclades and subfamilies ranging from short extinct truncated elements (SIDER) to long active elements (ingi). Important differences in ingi-related retroposon content have been reported between trypanosomatid species. For instance, Leishmania spp. have expanded and recycled a whole SIDER family to fulfill an important biological pathway, i.e., regulation of gene expression, while trypanosome genomes are primarily composed of active elements. Here, we present an overview of the computational methods used to identify, annotate, and analyze ingi-related retroposons for providing a comprehensive picture of all these TE families in newly available trypanosomatid genome sequences.
dc.language.isoENen_US
dc.subject.enAlgorithms
dc.subject.enDNA Transposable Elements
dc.subject.enEvolution
dc.subject.enMolecular
dc.subject.enGenome
dc.subject.enProtozoan
dc.subject.enGenomics
dc.subject.enMolecular Sequence Annotation
dc.subject.enPhylogeny
dc.subject.enRetroelements
dc.subject.enSoftware
dc.subject.enTrypanosomatina
dc.title.enIdentification and analysis of ingi-related retroposons in the trypanosomatid genomes.
dc.title.alternativeMethods Mol Biolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/978-1-4939-1438-8_6en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed25388110en_US
bordeaux.journalMethods in Molecular Biologyen_US
bordeaux.page109-22en_US
bordeaux.volume1201en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04269287
hal.version1
hal.date.transferred2023-11-03T10:06:16Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
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=Methods%20in%20Molecular%20Biology&rft.date=2015-01-01&rft.volume=1201&rft.spage=109-22&rft.epage=109-22&rft.eissn=1940-6029&rft.issn=1940-6029&rft.au=BRINGAUD,%20Frederic&ROGERS,%20Matthew&GHEDIN,%20Elodie&rft.genre=article


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