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.

Links