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dc.contributor.authorCampbell, J
dc.contributor.authorRyan, CJ
dc.contributor.authorLord, CJ
dc.date.accessioned2018-02-14T12:49:18Z
dc.date.issued2018-01-01
dc.identifier.citationMethods in molecular biology (Clifton, N.J.), 2018, 1711 pp. 83 - 99
dc.identifier.issn1064-3745
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1075
dc.identifier.eissn1940-6029
dc.identifier.doi10.1007/978-1-4939-7493-1_5
dc.description.abstractLoss-of-function screening using RNA interference or CRISPR approaches can be used to identify genes that specific tumor cell lines depend upon for survival. By integrating the results from screens in multiple cell lines with molecular profiling data, it is possible to associate the dependence upon specific genes with particular molecular features (e.g., the mutation of a cancer driver gene, or transcriptional or proteomic signature). Here, using a panel of kinome-wide siRNA screens in osteosarcoma cell lines as an example, we describe a computational protocol for analyzing loss-of-function screens to identify genetic dependencies associated with particular molecular features. We describe the steps required to process the siRNA screen data, integrate the results with genotypic information to identify genetic dependencies, and finally the integration of protein-protein interaction data to interpret these dependencies.
dc.formatPrint
dc.format.extent83 - 99
dc.languageeng
dc.language.isoeng
dc.publisherHUMANA PRESS INC
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectCell Line, Tumor
dc.subjectHumans
dc.subjectOsteosarcoma
dc.subjectBone Neoplasms
dc.subjectProtein Kinases
dc.subjectRNA, Small Interfering
dc.subjectGenomics
dc.subjectRNA Interference
dc.subjectGenotype
dc.subjectGene Dosage
dc.subjectMutation
dc.subjectSoftware
dc.subjectTranscriptome
dc.subjectProtein Interaction Maps
dc.titleIdentifying Genetic Dependencies in Cancer by Analyzing siRNA Screens in Tumor Cell Line Panels.
dc.typeJournal Article
dcterms.dateAccepted2017-12-19
rioxxterms.versionofrecord10.1007/978-1-4939-7493-1_5
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-01
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfMethods in molecular biology (Clifton, N.J.)
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Gene Function
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Gene Function
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Gene Function
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Gene Function
pubs.publication-statusPublished
pubs.volume1711
pubs.embargo.termsNot known
icr.researchteamGene Function
dc.contributor.icrauthorCampbell, James
dc.contributor.icrauthorLord, Christopher


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