mvGST

mvGST integrates one-sided p-values from a matrix using meta-analytic methods to identify differentially active Gene Ontology (GO) terms and gene sets across multiple contrasts.


Key Features:

  • Meta-Analytic Integration: mvGST combines one-sided p-values from an input matrix across all genes annotated to each gene set using meta-analytic methods.
  • Differential Activity Classification: mvGST classifies gene sets as significantly more active, less active, or not differentially active in each contrast based on combined p-values.
  • Profile Assignment: mvGST assigns each gene set to a specific differential-activity profile when multiple contrasts are analyzed.

Scientific Applications:

  • Gene set activity analysis: Identification of GO term or gene set activity changes across experimental contrasts in genomics and molecular biology studies.
  • Comparative analyses: Comparative assessment of differential activity between conditions such as disease versus healthy or treatment versus control.
  • Temporal and multi-condition studies: Profiling gene-set activity patterns across different time points or multiple experimental contrasts.

Methodology:

Combine one-sided p-values from a matrix across genes annotated to each gene set using meta-analytic methods, classify gene sets as more active/less active/not differentially active per contrast, and assign gene-set differential-activity profiles across multiple contrasts.

Topics

Collections

Details

License:
GPL-3.0
Tool Type:
command-line tool, library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
1/17/2017
Last Updated:
11/25/2024

Operations

Publications

Huber W, Carey VJ, Gentleman R, Anders S, Carlson M, Carvalho BS, Bravo HC, Davis S, Gatto L, Girke T, Gottardo R, Hahne F, Hansen KD, Irizarry RA, Lawrence M, Love MI, MacDonald J, Obenchain V, Oleś AK, Pagès H, Reyes A, Shannon P, Smyth GK, Tenenbaum D, Waldron L, Morgan M. Orchestrating high-throughput genomic analysis with Bioconductor. Nature Methods. 2015;12(2):115-121. doi:10.1038/nmeth.3252. PMID:25633503. PMCID:PMC4509590.

Documentation

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