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Transcriptome and genome sequencing uncovers functional variation in humans

dc.contributor.authorCarracedo Álvarez, Ángel
dc.date.accessioned2017-06-07T07:11:23Z
dc.date.available2017-06-07T07:11:23Z
dc.date.issued2013
dc.identifier.issn0028-0836
dc.identifier.urihttp://hdl.handle.net/20.500.11940/3608
dc.language.isoeng
dc.titleTranscriptome and genome sequencing uncovers functional variation in humans
dc.typeArtigoes
dc.authorsophosLappalainen, T.
dc.authorsophosSammeth, M.
dc.authorsophosFriedländer, M. R.
dc.authorsophosT Hoen, P. A. C.
dc.authorsophosMonlong, J.
dc.authorsophosRivas, M. A.
dc.authorsophosGonzàlez-Porta, M.
dc.authorsophosKurbatova, N.
dc.authorsophosGriebel, T.
dc.authorsophosFerreira, P. G.
dc.authorsophosBarann, M.
dc.authorsophosWieland, T.
dc.authorsophosGreger, L.
dc.authorsophosVan Iterson, M.
dc.authorsophosAlmlöf, J.
dc.authorsophosRibeca, P.
dc.authorsophosPulyakhina, I.
dc.authorsophosEsser, D.
dc.authorsophosGiger, T.
dc.authorsophosTikhonov, A.
dc.authorsophosSultan, M.
dc.authorsophosBertier, G.
dc.authorsophosMacarthur, D. G.
dc.authorsophosLek, M.
dc.authorsophosLizano, E.
dc.authorsophosBuermans, H. P. J.
dc.authorsophosPadioleau, I.
dc.authorsophosSchwarzmayr, T.
dc.authorsophosKarlberg, O.
dc.authorsophosOngen, H.
dc.authorsophosKilpinen, H.
dc.authorsophosBeltran, S.
dc.authorsophosGut, M.
dc.authorsophosKahlem, K.
dc.authorsophosAmstislavskiy, V.
dc.authorsophosStegle, O.
dc.authorsophosPirinen, M.
dc.authorsophosMontgomery, S. B.
dc.authorsophosDonnelly, P.
dc.authorsophosMcCarthy, M. I.
dc.authorsophosFlicek, P.
dc.authorsophosStrom, T. M.
dc.authorsophosLehrach, H.
dc.authorsophosSchreiber, S.
dc.authorsophosSudbrak, R.
dc.authorsophosCarracedo, Á
dc.authorsophosAntonarakis, S. E.
dc.authorsophosHäsler, R.
dc.authorsophosSyvänen, A. C.
dc.authorsophosVan Ommen, G. J.
dc.authorsophosBrazma, A.
dc.authorsophosMeitinger, T.
dc.authorsophosRosenstiel, P.
dc.authorsophosGuigó, R.
dc.authorsophosGut, I. G.
dc.authorsophosEstivill, X.
dc.authorsophosDermitzakis, E. T.
dc.identifier.doi10.1038/nature12531
dc.identifier.isi324826300049
dc.identifier.pmid24037378
dc.identifier.sophos13411
dc.issue.number7468
dc.journal.titleNATURE
dc.organizationConsellería de Sanidade::Fundación pública Galega de Medicina Xenómica
dc.page.initial506
dc.page.final511
dc.rights.accessRightsopenAccess
dc.typesophosArtículo Original
dc.volume.number501


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