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dc.contributor.authorWilliams, MJen_US
dc.contributor.authorWerner, Ben_US
dc.contributor.authorGraham, TAen_US
dc.contributor.authorSottoriva, Aen_US
dc.date.accessioned2016-10-18T11:10:06Z
dc.date.available2016-03-02en_US
dc.date.issued2016-07en_US
dc.date.submitted2016-09-29T11:06:03.567Z
dc.identifier.issn2372-3556en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/15910
dc.description.abstractNext-generation sequencing data from human cancers are often difficult to interpret within the context of tumor evolution. We developed a mathematical model describing the accumulation of mutations under neutral evolutionary dynamics and showed that 323/904 cancers (∼30%) from multiple types were consistent with the neutral model of tumor evolution.en_US
dc.format.extente1162897 - ?en_US
dc.languageengen_US
dc.relation.ispartofMol Cell Oncolen_US
dc.rightsThis is an Accepted Manuscript of an article published by Taylor & Francis Group in Molecular & Cellular Oncology on 22/04/2016, available online: http://www.tandfonline.com/10.1080/23723556.2016.1162897
dc.subjectCancer genomeen_US
dc.subjectintratumor heterogeneityen_US
dc.subjectmathematical modelen_US
dc.subjectmutation rateen_US
dc.subjectneutral expansionen_US
dc.subjectsite-frequency spectrumen_US
dc.titleFunctional versus non-functional intratumor heterogeneity in cancer.en_US
dc.typeArticle
dc.rights.holder(c) 2016 Taylor & Francis Group
dc.identifier.doi10.1080/23723556.2016.1162897en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/27652316en_US
pubs.issue4en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
pubs.volume3en_US
dcterms.dateAccepted2016-03-02en_US


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