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dc.contributor.authorWilliams, MJen_US
dc.contributor.authorSottoriva, Aen_US
dc.contributor.authorGraham, TAen_US
dc.date.accessioned2019-10-22T08:58:29Z
dc.date.available2019-02-08en_US
dc.date.issued2019-08-31en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/60546
dc.description.abstractCancers originate from somatic cells in the human body that have accumulated genetic alterations. These mutations modify the phenotype of the cells, allowing them to escape the homeostatic regulation that maintains normal cell number. Viewed through the lens of evolutionary biology, the transformation of normal cells into malignant cells is evolution in action. Evolution continues throughout cancer growth, progression, treatment resistance, and disease relapse, driven by adaptation to changes in the cancer's environment, and intratumor heterogeneity is an inevitable consequence of this evolutionary process. Genomics provides a powerful means to characterize tumor evolution, enabling quantitative measurement of evolving clones across space and time. In this review, we discuss concepts and approaches to quantify and measure this evolutionary process in cancer using genomics.en_US
dc.format.extent309 - 329en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofAnnu Rev Genomics Hum Geneten_US
dc.subjectcanceren_US
dc.subjectevolutionen_US
dc.subjectgenomicsen_US
dc.subjectpopulation geneticsen_US
dc.titleMeasuring Clonal Evolution in Cancer with Genomics.en_US
dc.typeArticle
dc.rights.holder© 2019 by Annual Reviews. All rights reserved
dc.identifier.doi10.1146/annurev-genom-083117-021712en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/31059289en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume20en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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