LURE
LURE identifies novel cancer driver events in TCGA and other multidimensional genomic datasets by associating gene expression signatures with mutation events using a semi-supervised learning framework.
Key Features:
- Semi-Supervised Learning: Employs a progressive label learning framework to iteratively refine predictions by leveraging both labeled (known) and unlabeled samples.
- Minimum Spanning Analysis: Uses minimum spanning analysis to identify connections between gene expression signatures across different samples.
- Expression–Mutation Association: Predicts cancer drivers by associating altered samples with known mutation events based on shared gene expression signatures.
- Large-Scale Dataset Application: Designed to operate on large-scale cancer genome projects such as The Cancer Genome Atlas (TCGA).
Scientific Applications:
- TCGA Analysis: Applied to TCGA datasets to identify high-confidence relationships between 53 novel and 18 known mutation events.
- Pathway Insights: Revealed connections involving TP53, telomere maintenance, and MAPK/RTK signaling pathways.
- Genetic Interaction Discovery: Uncovered alterations within the same gene, family, or pathway, indicating complex genetic interactions relevant to candidate targeted therapies.
Methodology:
Implements a progressive semi-supervised (label) learning framework together with minimum spanning analysis to associate gene expression signatures with known mutation events.
Topics
Details
- Tool Type:
- command-line tool
- Added:
- 11/14/2019
- Last Updated:
- 12/22/2020
Operations
Publications
Haan D, Tao R, Friedl V, Anastopoulos IN, Wong CK, Weinstein AS, Stuart JM. Using Transcriptional Signatures to Find Cancer Drivers with LURE. Unknown Journal. 2019. doi:10.1101/727891.
DOI: 10.1101/727891
Links
Repository
https://github.com/davidhaan/UCSC_LURE