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DRPPM-EASY: A Web-Based Framework for Integrative Analysis of Multi-Omics Cancer Datasets
Alyssa Obermayer1, Li Dong2, Qianqian Hu3
1Department of Biostatistics and Bioinformatics, H. Lee Moffitt Cancer Center, Tampa, FL 33612, USA.
Biology
|February 25, 2022
Summary
DR PPM-EASY simplifies complex multi-omics integration for cancer biology research. This R Shiny framework aids in analyzing transcriptomic and proteomic data, identifying key molecular signatures and pathways.
Area of Science:
- Cancer Biology
- Bioinformatics
- Genomics
Background:
- High-throughput omics analyses are crucial for cancer research.
- Integrating multi-omics data remains a significant challenge, often requiring extensive time and expertise.
Purpose of the Study:
- To develop an accessible R Shiny framework, DRPPM-EASY, for integrative multi-omics analysis.
- To demonstrate the utility of DRPPM-EASY in identifying molecular signatures and disruptions in cancer cell lines.
Main Methods:
- Development of DRPPM-EASY, an R Shiny framework for integrative multi-omics analysis.
- Application of the framework to RNA-seq and proteomic data from USP7 knockdown in T-cell acute lymphoblastic leukemia (T-ALL) cell lines.
- Creation of DRPPM-EASY-CCLE, a Shiny extension utilizing the Cancer Cell Line Encyclopedia (CCLE) for phenotype-based querying.
Main Results:
- Identification of an upregulated TAL1-associated proliferative signature in T-ALL cells post-USP7 knockdown.
- Concurrent analysis of transcriptome and proteome revealed disruption of protein degradation machinery and spliceosome.
- Verification of TP53-associated DNA damage signature in TP53-mutated ovarian cancer cells using DRPPM-EASY-CCLE.
Conclusions:
- DR PPM-EASY provides an open-source, user-friendly platform for multi-omics data exploration and discovery in cancer research.
- The framework facilitates the integration of transcriptomic and proteomic data, enabling identification of key biological insights.
- DR PPM-EASY-CCLE enhances data accessibility by integrating meta-information for phenotype-driven analysis.
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