Project Score database: a resource for investigating cancer cell dependencies and prioritizing therapeutic targets.
Project Score database: a resource for investigating cancer cell dependencies and prioritizing therapeutic targets.
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DOI:
10.1093/nar/gkaa882
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发表时间:
2021-01-08
影响因子:
14.9
通讯作者:
Garnett MJ
中科院分区:
文献类型:
--
作者:
Dwane L;Behan FM;Gonçalves E;Lightfoot H;Yang W;van der Meer D;Shepherd R;Pignatelli M;Iorio F;Garnett MJ
CRISPR genetic screens in cancer cell models are a powerful tool to elucidate oncogenic mechanisms and to identify promising therapeutic targets. The Project Score database (https://score.depmap.sanger.ac.uk/) uses genome-wide CRISPR–Cas9 dropout screening data in hundreds of highly annotated cancer cell models to identify genes required for cell fitness and prioritize novel oncology targets. The Project Score database currently allows users to investigate the fitness effect of 18 009 genes tested across 323 cancer cell models. Through interactive interfaces, users can investigate data by selecting a specific gene, cancer cell model or tissue type, as well as browsing all gene fitness scores. Additionally, users can identify and rank candidate drug targets based on an established oncology target prioritization pipeline, incorporating genetic biomarkers and clinical datasets for each target, and including suitability for drug development based on pharmaceutical tractability. Data are freely available and downloadable. To enhance analyses, links to other key resources including Open Targets, COSMIC, the Cell Model Passports, UniProt and the Genomics of Drug Sensitivity in Cancer are provided. The Project Score database is a valuable new tool for investigating genetic dependencies in cancer cells and the identification of candidate oncology targets.
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影响因子:
14.9
作者:
Lenoir WF;Lim TL;Hart T
通讯作者:
Hart T
影响因子:
14.9
作者:
Rauscher B;Heigwer F;Breinig M;Winter J;Boutros M
通讯作者:
Boutros M
影响因子:
14.9
作者:
Yang W;Soares J;Greninger P;Edelman EJ;Lightfoot H;Forbes S;Bindal N;Beare D;Smith JA;Thompson IR;Ramaswamy S;Futreal PA;Haber DA;Stratton MR;Benes C;McDermott U;Garnett MJ
通讯作者:
Garnett MJ
影响因子:
158.5
作者:
Jonker, Derek J.;O'Callaghan, Chris J.;Moore, Malcolm J.
通讯作者:
Moore, Malcolm J.
影响因子:
3
作者:
Hart T;Moffat J
通讯作者:
Moffat J