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dc.contributor.authorWilliams, MJ
dc.contributor.authorWerner, B
dc.contributor.authorGraham, TA
dc.contributor.authorSottoriva, A
dc.date.accessioned2017-03-01T12:26:09Z
dc.date.issued2016-07
dc.identifier.citationMolecular & cellular oncology, 2016, 3 (4), pp. e1162897 - ?
dc.identifier.issn2372-3556
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/443
dc.identifier.eissn2372-3556
dc.identifier.doi10.1080/23723556.2016.1162897
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.
dc.formatElectronic-eCollection
dc.format.extente1162897 - ?
dc.languageeng
dc.language.isoeng
dc.titleFunctional versus non-functional intratumor heterogeneity in cancer.
dc.typeJournal Article
dcterms.dateAccepted2016-03-02
rioxxterms.versionofrecord10.1080/23723556.2016.1162897
rioxxterms.licenseref.startdate2016-07
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfMolecular & cellular oncology
pubs.issue4
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR
pubs.publication-statusPublished
pubs.volume3
pubs.embargo.termsNot known
dc.contributor.icrauthorSottoriva, Andreaen


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