MinNetRank
MinNetRank is a computational method to address a critical challenge in oncology: the identification of personalized driver genes. These genes are key to unlocking the mysteries of cancer by serving as critical biomarkers and guiding the development of effective, personalized cancer therapies. MinNetRank's innovative approach lies in its ability to prioritize cancer genes with a high degree of precision and efficiency, setting it apart from existing methods in several significant ways.
Firstly, MinNetRank introduces a novel strategy for weighting different types of mutations, acknowledging that not all mutations contribute equally to cancer progression. This nuanced approach allows for a more accurate differentiation between driver genes, which play a pivotal role in cancer development, and passenger genes, which do not contribute to the disease process.
Furthermore, MinNetRank employs a sophisticated analysis of the interaction network surrounding these genes, considering both the incoming and outgoing connections. By evaluating the degree of interaction in this network, MinNetRank can identify genes that are more likely to be central to cancer development.
MinNetRank uses a minimum strategy to integrate multi-omics data. This approach allows for the prioritization of cancer genes across various types of biological data for each sample. By generating sample-specific rankings of genes, MinNetRank ensures that its predictions are personalized and relevant to each unique case of cancer.
Beyond identifying driver genes, MinNetRank's predictions have significant clinical implications. The top seven genes identified by MinNetRank have been shown to stratify patients into two subtypes with statistically significant survival differences across five types of cancer. These genes are not only markers of disease progression but are also associated with overall survival, underscoring their potential as targets for therapeutic intervention.
Topic
Oncology;Gene expression;Biomarkers;Genetic variation;Functional, regulatory and non-coding RNA;Omics
Detail
Operation: Standardisation and normalisation;Gene prediction;Enrichment analysis
Software interface: Library
Language: R
License: GNU Lesser General Public License >= version 2
Cost: Free with restrictions
Version name: 1.0
Credit: The National Natural Science Foundation of China and the Shanghai Jiao Tong University STAR Grant.
Input: -
Output: -
Contact: Zhangsheng Yu yuzhangsheng@sjtu.edu.cn
Collection: -
Maturity: -
Publications
- An Efficient and Easy-to-Use Network-Based Integrative Method of Multi-Omics Data for Cancer Genes Discovery.
- Wei T, et al. An Efficient and Easy-to-Use Network-Based Integrative Method of Multi-Omics Data for Cancer Genes Discovery. An Efficient and Easy-to-Use Network-Based Integrative Method of Multi-Omics Data for Cancer Genes Discovery. 2020; 11:613033. doi: 10.3389/fgene.2020.613033
- https://doi.org/10.3389/FGENE.2020.613033
- PMID: 33488678
- PMC: PMC7820902
Download and documentation
Documentation: https://github.com/weitinging/MinNetRank/blob/master/README.md
Home page: https://github.com/weitinging/MinNetRank
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