UNDO

UNDO performs unsupervised deconvolution of mixed gene expression data to separate tumor and stromal cell-specific expression profiles and estimate cellular proportions.


Key Features:

  • Unsupervised deconvolution: Separates mixed gene expression data into constituent cell-type signals without prior reference profiles.
  • Detection of marker genes (MGs): Automatically identifies cell-specific marker genes located on the scatter radii of mixed gene expression data.
  • Estimation of cellular proportions: Computes the relative proportions of different cell types in each mixed sample.
  • Reconstruction of cell-specific profiles: Deconvolutes mixed expressions to generate cell-type-specific gene expression profiles.
  • Data type compatibility: Applicable to microarray gene expression data and adaptable to other quantitative molecular profiling datasets.

Scientific Applications:

  • Analysis of heterogeneous tumor samples: Dissects cellular composition in samples containing multiple cell types such as tumor and stroma.
  • Tumor purity estimation: Estimates tumor purity in bulk gene expression datasets, including large-scale collections such as TCGA and CPTAC.
  • Validation across mixing proportions: Demonstrated performance across a wide range of tumor–stroma mixing proportions on biologically mixed benchmark datasets.

Methodology:

Unsupervised mathematical deconvolution that identifies marker genes on scatter radii of mixed gene expression, estimates cellular proportions, and reconstructs cell-specific expression profiles from bulk quantitative molecular profiling data.

Topics

Collections

Details

License:
GPL-2.0
Tool Type:
command-line tool, library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
1/17/2017
Last Updated:
11/25/2024

Operations

Data Inputs & Outputs

Publications

Wang N, Gong T, Clarke R, Chen L, Shih I, Zhang Z, Levine DA, Xuan J, Wang Y. UNDO: a Bioconductor R package for unsupervised deconvolution of mixed gene expressions in tumor samples. Bioinformatics. 2014;31(1):137-139. doi:10.1093/bioinformatics/btu607. PMID:25212756. PMCID:PMC4271149.

Documentation

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