IntOGen - Cancer Drivers Actionability Database
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- dc.contributor.author Rubio Pérez, Carlotaca
- dc.contributor.author Tamborero Noguera, Davidca
- dc.contributor.author Schroeder, Michael Philipp, 1986-ca
- dc.contributor.author Antolín Hernández, Albert, 1984-ca
- dc.contributor.author Déu Pons, Jordica
- dc.contributor.author Pérez Llamas, Christian, 1976-ca
- dc.contributor.author Mestres i López, Jordica
- dc.contributor.author González-Pérez, Abelca
- dc.contributor.author López Bigas, Núriaca
- dc.date.accessioned 2017-02-03T12:08:31Z
- dc.date.available 2017-02-03T12:08:31Z
- dc.date.issued 2015-03
- dc.description File contents/n-----------------/nProtein_Drug_Interactions.tsv/nInteractions of 96/475 cancer driver genes in Drivers Database with therapeutic agents/nProtein_druggability.tsv/nExclusvie druggability of 157/475 driver genes according interactions in Protein_Drug_Interactions.tsv/nDrug_details.tsv/nDescription of each drug/nDrug_FDAapproved_rules.tsv/nRules for prescription of FDA approved drugs to genomic alterations/nDrug_ClinicalTrials_rules.tsv/nRules for prescription of drugs in clinical trials to genomic alterations/nDrug_resistances_rules.tsv/nRules for not prescribing drugs to samples bearing genomic alterations of primary resistance/n/nSpecificities/n-----------------/n*In most of the files tumor types are represented through its acronyms (see Drivers Database)/n*Specific genomic dependencies/evidences/resistances are codified in the same unified code in the Columns () in the files (Drug_resistances_rules.tsv, Drug_FDAapproved_rules.tsv, Drug_ClinicalTrials_rules.tsv). /nThe coding rules are:/n- All of them are divided in mutations/CNAs/fusions. /n- For each one, different genes with alterations are semicolon (;) divided./n- Each gene differs from its alterions with colon(:) and its different alterations are comma (,) divided. /ni.e BRAF:V600E,V600K (two diferent alterations)/n- For CNAs A stants for Amplification and D for delention./ni.e. FGFR1:A/n- For mutations all of them are specified at protein level lik referenceAA+proteinposition+alteredAA./ni.e. BRAF:V600E,V600K/n except mutational requirements not based on AA change but specific consequence type, which are specified by ::CT:: after the gene./ni.e. NOTCH1::CT::missense_variant:2380-2445;CT::feature_truncation:2380-2445/n- Fusion partners are divided with dash (-)./ni.e. BCR-ABL1/n- A dot (.) represents any./ni.e. BRAF:V600. (any alteredAA)/ni.e. BRAF:. (any PAM mutation)ca
- dc.description.abstract This database contains data on the interactions with therapeutic agents an driver genes contained in Cancer Drivers Database (2014.12). It characterizes the interacting therapeutic agents in terms of clinical phase and cancer prescription, among other features. Additionally, it contains ancillary information on specific genomic alterations associated to drug effectiveness which are FDA approved or clinically being tested together with data on other genomic alterations known to be responsible of drug primary resistance.ca
- dc.format.mimetype application/pdfca
- dc.identifier.uri http://hdl.handle.net/10230/28050
- dc.language.iso engca
- dc.publisher Universitat Pompeu Fabraca
- dc.relation Més informació: IntOGen (web)
- dc.relation Rubio-Perez C, Tamborero D, Schroeder MP, Aantolín AA, Deu-Pons J, Perez-Llamas C, Mestres J, Gonzalez-Perez A, Lopez-Bigas N. In silico prescription of anticancer drugs to cohorts of 28 tumor types reveals targeting opportunities. Cancer Cell. 2015; 27(3): 382-96. DOI: 10.1016/j.ccell.2015.02.007
- dc.relation.isreferencedby http://dx.doi.org/10.1016/j.ccell.2015.02.007
- dc.relation.uri https://www.intogen.org/downloads
- dc.rights Universitat Pomper Fabra License Agreement. Consulteu les condicions d'ús específiques dins del documentca
- dc.rights.accessRights info:eu-repo/semantics/openAccessca
- dc.rights.uri http://www.intogen.org/terms
- dc.subject.keyword Cancer driver
- dc.subject.keyword Biomarkers
- dc.subject.keyword Drugs database
- dc.title IntOGen - Cancer Drivers Actionability Databaseca
- dc.type info:eu-repo/semantics/otherca
- dc.type Dataset