TIRSF
TIRSF identifies and applies gene expression signatures to predict responses to immune checkpoint blockade (ICB) therapy in cancer patients.
Key Features:
- Signature Discovery Module: Constructs gene signatures tailored to predict responses to immune checkpoint blockade (ICB) therapy and evaluates their performance.
- Response Prediction Based on TIRSF Signatures: Applies constructed signatures to immunotherapy samples to predict response and perform prognostic analyses.
- Integration of Existing Signatures: Incorporates 24 published gene signatures for ICB therapy response prediction for application to new datasets.
Scientific Applications:
- Patient stratification: Identifies patient subsets more likely to respond to ICB therapy based on gene expression signatures.
- Predictive biomarker development: Facilitates development and evaluation of gene-expression-based biomarkers for ICB response.
- Prognostic analysis: Enables prognostic assessments of clinical outcomes using applied signatures.
Methodology:
Signature construction, performance evaluation, application of signatures to immunotherapy samples for response prediction and prognostic analysis, and integration of 24 published ICB gene signatures.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Mac, Windows, Linux
- Added:
- 8/16/2022
- Last Updated:
- 11/24/2024
Operations
Publications
Chen L, Chen T, Zhang Y, Lin H, Wang R, Wang Y, Li H, Zuo Z, Ren J, Xie Y. TIRSF: a web server for screening gene signatures to predict Tumor immunotherapy response. Nucleic Acids Research. 2022;50(W1):W761-W767. doi:10.1093/nar/gkac374. PMID:35554556. PMCID:PMC9252797.
DOI: 10.1093/nar/gkac374
PMID: 35554556
PMCID: PMC9252797
Funding: - National Natural Science Foundation of China: 31771462, 31801105, 81772614, 81802438, U1611261
- National Key Research and Development Program of China: 2017YFA0106700
- Program for Guangdong Introducing Innovative and Entrepreneurial Teams: 2017ZT07S096
- Guangdong Basic and Applied Basic Research Foundation: 2020A1515010220