categoryCompare

categoryCompare compares annotation-level results from high-throughput omics datasets to identify shared and distinct biological annotations across measurement platforms.


Key Features:

  • Annotation-Level Comparison: Assesses annotations (e.g., known or predicted functions and associations) of features to enable cross-platform and cross-sample comparison of biological processes and signaling pathways.
  • Significance Calculation and Overlap Detection: Calculates significant annotations for each feature list (e.g., gene lists) and determines overlaps between these annotations, with graphical and tabular outputs illustrating annotation combinations across lists.
  • RCytoscape Integration: Exports annotation networks compatible with RCytoscape for network visualization.
  • Platform Heterogeneity Handling: Uses annotation-level analysis to evaluate common biological processes across studies even when individual features are not consistently measured.

Scientific Applications:

  • Denervated Skin vs. Denervated Muscle: Comparison of annotation-level responses to reveal distinct tissue-specific biological reactions.
  • Crohn’s Disease vs. Ulcerative Colitis (UC): Identification of shared inflammatory responses and processes unique to each condition from annotation-level analyses.

Methodology:

Calculates significant annotations per feature list and determines annotation overlaps; assesses utility using hypothetical and real datasets; analytical factors explicitly considered include number of genes per annotation term, noise levels in unenriched categories, and methods for combining samples.

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:
1/10/2019

Operations

Publications

Flight RM, Harrison BJ, Mohammad F, Bunge MB, Moon LDF, Petruska JC, Rouchka EC. categoryCompare, an analytical tool based on feature annotations. Frontiers in Genetics. 2014;5. doi:10.3389/fgene.2014.00098. PMID:24808906. PMCID:PMC4010757.

Documentation

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