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dc.contributor.authorFernandes Alves, Joao Miguel 
dc.contributor.authorPrieto Fernandez, Tamara 
dc.contributor.authorPosada González, David 
dc.date.accessioned2022-04-21T07:21:27Z
dc.date.available2022-04-21T07:21:27Z
dc.date.issued2017-08
dc.identifier.citationTrends in Cancer, 3(8): 546-550 (2017)spa
dc.identifier.issn24058033
dc.identifier.urihttp://hdl.handle.net/11093/3408
dc.description.abstractTumor samples most often comprise a mixture of different cell lineages. Multiregional trees built from bulk mutational profiles do not consider this heterogeneity and can potentially lead to erroneous evolutionary inferences, including biased timing of somatic mutations, spurious parallel mutation events, and/or incorrect chronological ordering of metastatic events.en
dc.language.isoengen
dc.publisherTrends in Cancerspa
dc.titleMultiregional tumor trees are not phylogeniesen
dc.typearticlespa
dc.rights.accessRightsopenAccessspa
dc.identifier.doi10.1016/j.trecan.2017.06.004
dc.identifier.editorhttps://linkinghub.elsevier.com/retrieve/pii/S2405803317301218spa
dc.publisher.departamentoBioquímica, xenética e inmunoloxíaspa
dc.publisher.grupoinvestigacionXenómica e Biomedicinaspa
dc.subject.unesco2409 Genéticaspa
dc.subject.unesco2409.03 Genética de Poblacionesspa
dc.date.updated2022-04-21T07:17:26Z
dc.computerCitationpub_title=Trends in Cancer|volume=3|journal_number=8|start_pag=546|end_pag=550spa


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