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Published on: May 17, 2019
OncoDB 2.0: a comprehensive platform for integrated pan-cancer omics analysis
Minsu Cho1,2, Gongyu Tang1, Charles S Rogers1
1Department of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL 60612, United States.
OncoDB 2.0 enhances cancer research by integrating multi-omics data, including somatic mutations and proteomic profiles. This expanded platform aids in exploring complex cancer biology and identifying novel therapeutic targets.
Area of Science:
- Genomics
- Proteomics
- Cancer Biology
Background:
- The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) datasets provide valuable multi-omics data for cancer research.
- Previous versions of OncoDB integrated RNA expression, DNA methylation, and clinical data.
- A comprehensive, integrated platform is needed to explore complex cancer omics data.
Purpose of the Study:
- To present OncoDB 2.0, an expanded platform for integrated cancer multi-omics analysis.
- To incorporate somatic mutation, proteomic, and chromatin accessibility data.
- To provide advanced analysis modules for exploring cross-omic relationships.
Main Methods:
- Integrated RNA sequencing, DNA sequencing, and DNA methylation data.
- Incorporated proteomic data from the Clinical Proteomic Tumor Analysis Consortium (CPTAC).
- Added chromatin accessibility data from TCGA.
- Developed advanced multi-omics analysis modules.
Main Results:
- OncoDB 2.0 provides an atlas of somatic mutations across tumor types.
- The platform enables investigation of mutation patterns and clinical feature associations.
- New dimensions for oncogene regulation studies are offered through integrated proteomic and chromatin accessibility data.
- Advanced modules facilitate combined exploration of RNA expression, DNA methylation, and somatic mutations.
Conclusions:
- OncoDB 2.0 offers a comprehensive and integrated view of cancer omics data.
- The platform facilitates in-depth investigation of mutation patterns and their clinical relevance.
- OncoDB 2.0 is a robust tool for cancer research, enabling deeper exploration of cross-omic relationships.
- The platform is freely available to the research community.
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