survClust

survClust performs outcome-weighted supervised clustering to integrate somatic mutations, DNA copy number, DNA methylation, mRNA, miRNA, and protein data with survival endpoints (Overall Survival, Progression-Free Survival) to identify prognostic molecular subtypes across TCGA pan-cancer datasets.


Key Features:

  • Outcome-Weighted Integration: Leverages survival data (Overall Survival, Progression-Free Survival) to weight molecular features and guide clustering.
  • Supervised Clustering: Implements an outcome-weighted supervised clustering algorithm drawing inspiration from supervised text classification techniques.
  • Multi-Omics Data Utilization: Processes somatic mutations, DNA copy number variations, DNA methylation, and expression profiles at the mRNA, miRNA, and protein levels.
  • Pan-Cancer Application: Applied across 18 cancer types using data from The Cancer Genome Atlas (TCGA).
  • Novel Prognostic Subtype Identification: Identifies prognostic subtypes, including groups characterized by high tumor mutation burden with elevated CD8 T cell immune marker expression and aggressive subtypes associated with CDKN2A deletion.
  • Visualization Techniques: Incorporates visualization such as circomap to display somatic alterations at genome-wide and individual gene levels.

Scientific Applications:

  • Patient Stratification: Identifies survival-associated molecular subtypes for stratifying cancer patients.
  • Translational Research: Links molecular profiles to clinical outcomes to support translational research efforts.
  • Precision Oncology: Provides prognostic subtype information that can inform personalized treatment strategies and clinical decision-making.

Methodology:

survClust implements an outcome-weighted supervised clustering algorithm that leverages survival endpoints (Overall Survival, Progression-Free Survival), draws inspiration from supervised text classification techniques, and integrates somatic mutations, DNA copy number, DNA methylation, mRNA, miRNA, and protein expression data.

Topics

Details

Programming Languages:
R, C++
Added:
1/18/2021
Last Updated:
2/24/2021

Operations

Publications

Arora A, Olshen AB, Seshan VE, Shen R. Pan-cancer identification of clinically relevant genomic subtypes using outcome-weighted integrative clustering. Genome Medicine. 2020;12(1). doi:10.1186/s13073-020-00804-8. PMID:33272320. PMCID:PMC7716509.

PMID: 33272320
PMCID: PMC7716509
Funding: - National Cancer Institute: P01 CA206980, P30 CA008748 54, P30CA082103