ClinicalOmicsDB: exploring molecular associations of oncology drug responses in clinical trials.
ClinicalOmicsDB: exploring molecular associations of oncology drug responses in clinical trials.
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ClinicalOmicsDB:探索临床试验中肿瘤药物反应的分子相关性。
DOI:
10.1093/nar/gkad871
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发表时间:
2024-01-05
影响因子:
14.9
通讯作者:
Zhang B
中科院分区:
文献类型:
--
作者:
Moon CI;Elizarraras JM;Lei JT;Jia B;Zhang B
Matching patients to optimal treatment is challenging, in part due to the limited availability of real-world clinical datasets for predictive biomarker identification. The growing integration of omics profiling into clinical trials presents a new opportunity to tackle this challenge. Here, we introduce ClinicalOmicsDB, a web application for exploring molecular associations of oncology drug responses in clinical trials. This database includes transcriptomic data from 40 clinical trial studies, with 5913 patients spanning 11 cancer types. These studies include 67 treatment arms with a variety of chemotherapy, targeted therapy and immunotherapy drugs, and their combinations, which we organize based on an established ontology for easier navigation. The web application provides users with three options to explore molecular associations of oncology drug responses, focusing on studies, treatments or genes, respectively. Gene set analysis further connects treatment response to pathway activity and tumor microenvironment attributes. The user-friendly web interface of ClinicalOmicsDB streamlines interactive analysis. A Rust-based backend speeds up response time, and application programming interfaces and an R package enable programmatic access. We use three case studies to demonstrate the utility of this resource in human cancer studies. ClinicalOmicsDB is freely available at http://trials.linkedomics.org/.
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影响因子:
14.9
作者:
Gene Ontology Consortium
通讯作者:
Gene Ontology Consortium
影响因子:
7.7
作者:
Racle J;de Jonge K;Baumgaertner P;Speiser DE;Gfeller D
通讯作者:
Gfeller D
影响因子:
8.4
作者:
Eisenhauer, E. A.;Therasse, P.;Verweij, J.
通讯作者:
Verweij, J.
影响因子:
14.9
作者:
Martens M;Ammar A;Riutta A;Waagmeester A;Slenter DN;Hanspers K;A Miller R;Digles D;Lopes EN;Ehrhart F;Dupuis LJ;Winckers LA;Coort SL;Willighagen EL;Evelo CT;Pico AR;Kutmon M
通讯作者:
Kutmon M
影响因子:
28.5
作者:
Zhu S;Zhang T;Zheng L;Liu H;Song W;Liu D;Li Z;Pan CX
通讯作者:
Pan CX