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dc.contributor.authorGonzález-de la Fuente, Sandra
dc.contributor.authorPeiró-Pastor, Ramón
dc.contributor.authorRastrojo, Alberto
dc.contributor.authorMoreno, Javier 
dc.contributor.authorCarrasco-Ramiro, Fernando
dc.contributor.authorRequena, Jose M
dc.contributor.authorAguado, Begoña
dc.date.accessioned2019-02-19T14:59:53Z
dc.date.available2019-02-19T14:59:53Z
dc.date.issued2017-12-22
dc.identifier.citationSci Rep. 2017 Dec 22;7(1):18050.es_ES
dc.identifier.issn2045-2322es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/7184
dc.description.abstractLeishmania parasites are the causative of leishmaniasis, a group of potentially fatal human diseases. Control strategies for leishmaniasis can be enhanced by genome based investigations. The publication in 2005 of the Leishmania major genome sequence, and two years later the genomes for the species Leishmania braziliensis and Leishmania infantum were major milestones. Since then, the L. infantum genome, although highly fragmented and incomplete, has been used widely as the reference genome to address whole transcriptomics and proteomics studies. Here, we report the sequencing of the L. infantum genome by two NGS methodologies and, as a result, the complete genome assembly on 36 contigs (chromosomes). Regarding the present L. infantum genome-draft, 495 new genes have been annotated, a hundred have been corrected and 75 previous annotated genes have been discontinued. These changes are not only the result of an increase in the genome size, but a significant contribution derives from the existence of a large number of incorrectly assembled regions in current chromosomal scaffolds. Furthermore, an improved assembly of tandemly repeated genes has been obtained. All these analyses support that the de novo assembled L. infantum genome represents a robust assembly and should replace the currently available in the databases.es_ES
dc.description.sponsorshipThis work was supported by grants from Proyecto del Ministerio de Economía y Competitividad (SAF2013-47556-R, co-financed with FEDER funds), and the Fondo de Investigaciones Sanitarias (ISCIII-RETIC RD16/0027/0008-FEDER). The CBMSO receives institutional grants from the Fundación Ramón Areces and from the Fundación Banco de Santander.es_ES
dc.language.isoenges_ES
dc.publisherNature Publishing Group es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleResequencing of the Leishmania infantum (strain JPCM5) genome and de novo assembly into 36 contigses_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID29273719es_ES
dc.format.volume7es_ES
dc.format.number1es_ES
dc.format.page18050es_ES
dc.identifier.doi10.1038/s41598-017-18374-yes_ES
dc.contributor.funderMinisterio de Economía y Competitividad (España) 
dc.contributor.funderInstituto de Salud Carlos III 
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF) 
dc.description.peerreviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41598-017-18374-yes_ES
dc.identifier.journalScientific reportses_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2013-47556-Res_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0027/0008es_ES
dc.rights.accessRightsopen accesses_ES


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Atribución 4.0 Internacional
Este Item está sujeto a una licencia Creative Commons: Atribución 4.0 Internacional