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Published on: June 21, 2018
webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study
Chen Cao1,2,3, Jianhua Wang4, Devin Kwok5
1Yangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.
webTWAS is a new resource that lists 235,064 gene-disease associations identified through transcriptome-wide association studies (TWAS). It integrates GWAS data and TWAS software to help researchers find causal genes for various human diseases.
Area of Science:
- Genetics
- Bioinformatics
- Computational Biology
Background:
- Transcriptome-wide association studies (TWAS) are crucial for identifying causal genes in diseases.
- Existing resources lack comprehensive TWAS-derived gene-disease associations from GWAS summary statistics.
- Conducting TWAS is challenging due to complex software pipelines.
Purpose of the Study:
- To introduce webTWAS, a novel resource consolidating GWAS datasets and TWAS findings.
- To provide a comprehensive database of gene-disease associations discovered via TWAS.
- To simplify the process of identifying potential causal genes for human diseases.
Main Methods:
- Integrated 1298 high-quality European GWAS summary statistics with multiple TWAS software packages.
- Calculated 235,064 gene-disease associations using seven statistical models and three TWAS software packages.
- Implemented tissue-specific enrichment analysis and a user-friendly web server for custom analyses.
Main Results:
- Compiled a database of 235,064 gene-disease associations across a wide range of human diseases.
- Prioritized associations from extensive GWAS summary statistics, enhancing credibility.
- Identified significant tissues for disease associations through enrichment analysis.
Conclusions:
- webTWAS offers a valuable, comprehensive resource for exploring TWAS-identified gene-disease associations.
- The platform simplifies gene-disease association discovery and facilitates custom TWAS analyses.
- webTWAS enhances research into the genetic underpinnings of human diseases.
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