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Validation of Clinically Relevant Variant Detection from Whole Genome Sequencing for NHS England's Genomic Medicine Service

dc.contributor.authorKasperaviciute, Den_US
dc.contributor.authorSmith, KRen_US
dc.contributor.authorIbanez, Ken_US
dc.contributor.authorPasko, Den_US
dc.contributor.authorBleda, Men_US
dc.contributor.authorWalker, Sen_US
dc.contributor.authorPolychronopoulos, Den_US
dc.contributor.authorMartin, ARen_US
dc.contributor.authorKayikci, Men_US
dc.contributor.authorLopez, Jen_US
dc.contributor.authorThomas, Een_US
dc.contributor.authorBaple, Een_US
dc.contributor.authorTucci, Aen_US
dc.contributor.authorScott, RHen_US
dc.contributor.authorPolke, Jen_US
dc.contributor.authorLabrum, Ren_US
dc.contributor.authorSantos, Len_US
dc.contributor.authorEggleton, Ken_US
dc.contributor.authorMcmullan, Den_US
dc.contributor.authorMorrogh, Den_US
dc.contributor.authorAhn, JWen_US
dc.contributor.authorDeans, Zen_US
dc.contributor.authorHill, Sen_US
dc.contributor.authorCaulfield, MJen_US
dc.contributor.authorRendon, Aen_US
dc.contributor.authorConsortium, GERen_US
dc.date.accessioned2021-03-24T14:28:49Z
dc.date.available2021-03-24T14:28:49Z
dc.date.issued2020-12en_US
dc.identifier.issn1018-4813en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/70844
dc.format.extent640 - 641en_US
dc.titleValidation of Clinically Relevant Variant Detection from Whole Genome Sequencing for NHS England's Genomic Medicine Serviceen_US
dc.typeConference Proceeding
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000598482602198&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issueSUPPL 1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume28en_US


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