GUST

"GUST" (Genes Under Selection in Tumors) is a computational method to identify oncogenes (OGs) and tumor-suppressor genes (TSGs) in a cancer-type specific manner. Recognizing the substantial variability in the functions of cancer driver genes across different tissues and organs, GUST offers a solution to distinguish between passenger genes, OGs, and TSGs, thereby facilitating a deeper understanding of tumor biology and aiding in identifying clinically actionable targets.

Key Features and Functionalities:

- Cancer-Type Specific Analysis: GUST is developed to discover OGs and TSGs with high tissue specificity, addressing the need for context-aware classifications of cancer driver genes.

- Differentiation of Mutation Patterns: The method is based on the observation that the direction and magnitude of somatic selection for protein-coding mutations significantly differ among passenger genes, OGs, and TSGs. This insight allows for accurate differentiation of these gene categories.

High Accuracy: When evaluated through strict cross-validation procedures, GUST demonstrates high accuracy (92%) in identifying OGs and TSGs, underscoring its reliability and effectiveness.

Topic

Oncology;Exome sequencing;Genomics;Genetic variation

Detail

  • Operation: Gene prediction;Variant calling;Aggregation

  • Software interface: Library

  • Language: R

  • License: Open Source

  • Cost: Free of charge

  • Version name: 0.1

  • Credit: Yhe National Institutes of Health, the Flinn Foundation, the Mayo Clinic, Arizona State University Alliance for Health Care.

  • Input: -

  • Output: -

  • Contact: Li Liu liliu@asu.edu

  • Collection: -

  • Maturity: -

Publications

  • Somatic selection distinguishes oncogenes and tumor suppressor genes.
  • Chandrashekar P, et al. Somatic selection distinguishes oncogenes and tumor suppressor genes. Somatic selection distinguishes oncogenes and tumor suppressor genes. 2020; 36:1712-1717. doi: 10.1093/bioinformatics/btz851
  • https://doi.org/10.1093/BIOINFORMATICS/BTZ851
  • PMID: 32176769
  • PMC: PMC7703750

Download and documentation


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